https://recallregister.com/New recalls from NHTSA, CPSC and FDA, with the date that the agency gives.enTue, 29 Sep 2026 12:00:00 GMThttps://recallregister.com/vehicle/nova-bus/lfs/2023/#26V624000recallregister:campaign:26V624000Tue, 29 Sep 2026 12:00:00 GMTNHTSA campaign 26V624000. NHTSA received the report on 29 Sep 2026. Manufacturer: Nova Bus (US) Inc. Units: 18. Defect, in the NHTSA record: "Nova Bus (US) Inc. (Nova Bus) is recalling certain 2022-2023 LFS transit buses. The mounting screws may be too short, stripping the threads and causing the bike rack to detach."https://recallregister.com/equipment/other/cummins/#26E066000recallregister:campaign:26E066000Mon, 28 Sep 2026 12:00:00 GMTNHTSA campaign 26E066000. NHTSA received the report on 28 Sep 2026. Manufacturer: Cummins, Inc. Units: 39,052. Defect, in the NHTSA record: "Cummins, Inc. (Cummins) is recalling certain L9 diesel engines, part number D563027BX03. The remote fuel filter hoses may separate from the fitting, causing a fuel leak and an engine stall."https://recallregister.com/vehicle/volvo/vnr-4/2027/#26V619000recallregister:campaign:26V619000Mon, 28 Sep 2026 12:00:00 GMTNHTSA campaign 26V619000. NHTSA received the report on 28 Sep 2026. Manufacturer: Volvo Trucks North America. Units: 392. Defect, in the NHTSA record: "Volvo Trucks North America (Volvo Trucks) is recalling certain 2025-2027 VNL (4) and 2026-2027 VNR (4) vehicles equipped with a tanker application package. Inaccurate axle load calculations may cause reduced braking performance while transporting smoothbore tanker trailers."https://recallregister.com/vehicle/mack/anthem-an-4/2027/#26V620000recallregister:campaign:26V620000Mon, 28 Sep 2026 12:00:00 GMTNHTSA campaign 26V620000. NHTSA received the report on 28 Sep 2026. Manufacturer: Mack Trucks, Inc. Units: 850. Defect, in the NHTSA record: "Mack Trucks, Inc. (Mack) is recalling certain 2026-2027 Anthem AN (4) and Pioneer PR (4) vehicles equipped with a tanker application package. Inaccurate axle load calculations may cause reduced braking performance while transporting smoothbore tanker trailers."https://recallregister.com/vehicle/chevrolet/silverado-1500/2017/#26V611000recallregister:campaign:26V611000Thu, 24 Sep 2026 12:00:00 GMTNHTSA campaign 26V611000. NHTSA received the report on 24 Sep 2026. Manufacturer: General Motors, LLC. Units: 1,559. Defect, in the NHTSA record: "General Motors, LLC (GM) is recalling certain 2016 Chevrolet Silverado 2500/3500, GMC Sierra 2500/3500 vehicles, and 2016-2017 Chevrolet Silverado 1500 and GMC Sierra 1500 vehicles. The left-side or right-side roof rail air bag (RRAB) inflator end cap may detach from the inflator or the inflator sidewall may rupture."https://recallregister.com/vehicle/cadillac/optiq/2026/#26V612000recallregister:campaign:26V612000Thu, 24 Sep 2026 12:00:00 GMTNHTSA campaign 26V612000. NHTSA received the report on 24 Sep 2026. Manufacturer: General Motors, LLC. Units: 29,347. Defect, in the NHTSA record: "General Motors, LLC (GM) is recalling certain 2025-2027 Cadillac OPTIQ vehicles. When closed using the key fob's express-up function, the front windows may fail to detect an obstruction and reverse direction. As such, these vehicles fail to conform to Federal Motor Vehicle Safety Standard (FMVSS) number 118, "Power-Operated Window Systems.""https://recallregister.com/vehicle/land-rover/range-rover-sport/2026/#26V613000recallregister:campaign:26V613000Thu, 24 Sep 2026 12:00:00 GMTNHTSA campaign 26V613000. NHTSA received the report on 24 Sep 2026. Manufacturer: Jaguar Land Rover North America, LLC. Units: 1,073. Defect, in the NHTSA record: "Jaguar Land Rover North America, LLC (Land Rover) is recalling certain 2024-2026 Range Rover Sport vehicles. Cracks may develop in the rear subframe."https://recallregister.com/vehicle/land-rover/defender/2024/#26V615000recallregister:campaign:26V615000Thu, 24 Sep 2026 12:00:00 GMTNHTSA campaign 26V615000. NHTSA received the report on 24 Sep 2026. Manufacturer: Jaguar Land Rover North America, LLC. Units: 371. Defect, in the NHTSA record: "Jaguar Land Rover North America, LLC (Land Rover) is recalling certain 2024 Land Rover Defender vehicles. The second-row seat belt may be improperly stitched."https://recallregister.com/vehicle/grand-design/reflection/2026/#26V616000recallregister:campaign:26V616000Thu, 24 Sep 2026 12:00:00 GMTNHTSA campaign 26V616000. NHTSA received the report on 24 Sep 2026. Manufacturer: Grand Design RV, LLC. Units: 16,128. Defect, in the NHTSA record: "Grand Design RV, LLC (Grand Design) is recalling certain 2024-2027 Reflection fifth wheel recreational trailers. The auto detect solar controller may select a 24 volt output when the electrical system is designed for 12 volts. The incorrect voltage may damage the 7-way bulkhead power center and other circuits."https://recallregister.com/product/10991-zck01-recalls-kesyup-mattresses-due-to-risk-of-serious-injury-or-death/recallregister:product:10991Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26788. Recall date: 24 Sep 2026. Firm: S-Q Business (HK) Limited, dba ZCK01. Units: 48,405. Hazard, in the words of CPSC: "The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire."https://recallregister.com/product/10992-5color-recalls-children-s-bicycle-helmet-and-pads-sets-due-to-risk-of/recallregister:product:10992Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26789. Recall date: 24 Sep 2026. Firm: 5Color. Units: 324. Hazard, in the words of CPSC: "The helmets in the recalled sets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, retention system, positional stability, labeling and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury."https://recallregister.com/product/10993-style-homeware-recalls-emerspring-mattresses-due-to-risk-of-serious-in/recallregister:product:10993Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26796. Recall date: 24 Sep 2026. Units: 263. Hazard, in the words of CPSC: "The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire."https://recallregister.com/product/10994-xinan-home-recalls-winxmatrs-mattresses-due-to-risk-of-serious-injury/recallregister:product:10994Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26793. Recall date: 24 Sep 2026. Firm: Huizhou Xiqijun Trading Co., Ltd, dba Xinan Home. Units: 792. Hazard, in the words of CPSC: "The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire."https://recallregister.com/product/10995-inmo-international-technology-limited-recalls-inmo-air3-smart-glasses/recallregister:product:10995Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26797. Recall date: 24 Sep 2026. Firm: INMO International Technology. Units: 1,643. Hazard, in the words of CPSC: "The left temple of the recalled smart glasses can overheat during extended use, posing a risk of serious injury or death due to burn hazard."https://recallregister.com/product/10996-hyperfuels-recalls-methanol-and-ethanol-fuel-containers-due-to-risk-of/recallregister:product:10996Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26790. Recall date: 24 Sep 2026. Firm: Hyperfuels. Units: 124. Hazard, in the words of CPSC: "The recalled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the Portable Fuel Container Safety Act, posing a deadly flame jetting hazard. Furthermore, the methanol container is not child-resistant as required under the Poison Prevention Packaging Act, posing a risk of serious injury or death if the contents are swallowed by young children. The containers also do not comply with the labeling requirements of the Federal Hazardous Substances Act."https://recallregister.com/product/10997-the-blue-cactus-company-reclining-chair-battery-packs-recalled-due-to/recallregister:product:10997Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26791. Recall date: 24 Sep 2026. Firm: Go North Rocket 28 AB. Units: 51,000. Hazard, in the words of CPSC: "The lithium-ion battery in the recalled battery packs can overheat, posing fire and burn hazards to consumers."https://recallregister.com/product/10998-yuyitop-recalls-aitjunz-8-drawer-dressers-due-to-risk-of-serious-injur/recallregister:product:10998Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26794. Recall date: 24 Sep 2026. Firm: Dongguan Meiying Sen Smart Home. Units: 25,073. Hazard, in the words of CPSC: "The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standards as required by the STURDY Act."https://recallregister.com/product/10999-abc-trading-recalls-light-up-children-s-toys-due-to-risk-of-serious-in/recallregister:product:10999Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26799. Recall date: 24 Sep 2026. Firm: ABC Trading. Units: 43,674. Hazard, in the words of CPSC: "The recalled children’s toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries can be easily accessed by children, posing a deadly ingestion hazard to children. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death."https://recallregister.com/product/11000-newdery-power-banks-recalled-due-to-fire-and-burn-hazards-risk-of-seri/recallregister:product:11000Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26792. Recall date: 24 Sep 2026. Firm: Shenzhen Xinkewangda Electronics Co., Ltd., d/b/a NEWDERY. Units: 21,380. Hazard, in the words of CPSC: "The lithium-ion battery in the power banks can explode or ignite, posing fire and burn hazards to consumers."https://recallregister.com/product/11001-love-to-dream-recalls-portable-sleep-machines-due-to-risk-of-injury-fr/recallregister:product:11001Thu, 24 Sep 2026 12:00:00 GMTCPSC recall 26798. Recall date: 24 Sep 2026. Firm: Love To Dream. Units: 4,000. Hazard, in the words of CPSC: "The lithium-ion battery in the recalled portable sleep machines can overheat if the charger is not compatible with the unit, posing a risk of injury from fire and burn hazards."https://recallregister.com/vehicle/land-rover/range-rover-sport/2026/#26V607000recallregister:campaign:26V607000Wed, 23 Sep 2026 12:00:00 GMTNHTSA campaign 26V607000. NHTSA received the report on 23 Sep 2026. Manufacturer: Jaguar Land Rover North America, LLC. Units: 1. Defect, in the NHTSA record: "Jaguar Land Rover North America, LLC (Land Rover) is recalling one 2026 Range Rover Sport vehicle. The circuit board in the powertrain control module (PCM) was misaligned during production and may be deformed."https://recallregister.com/vehicle/forest-river/cedar-creek/2026/#26V608000recallregister:campaign:26V608000Wed, 23 Sep 2026 12:00:00 GMTNHTSA campaign 26V608000. NHTSA received the report on 23 Sep 2026. Manufacturer: Forest River, Inc. Units: 132. Defect, in the NHTSA record: "Forest River, Inc. (Forest River) is recalling certain 2025-2026 Cedar Creek fifth wheel recreational trailers. The sleeper sofa may block the bunkroom door."https://recallregister.com/vehicle/dynamax/isata/2027/#26V609000recallregister:campaign:26V609000Wed, 23 Sep 2026 12:00:00 GMTNHTSA campaign 26V609000. NHTSA received the report on 23 Sep 2026. Manufacturer: Forest River, Inc. Units: 111. Defect, in the NHTSA record: "Forest River, Inc. (Forest River) is recalling certain 2026-2027 Dynamax Isata recreational vehicles. The bunk ladder may be attached to a wooden mattress insert, resulting in the ladder loosening."https://recallregister.com/vehicle/dynamax/isata/2027/#26V610000recallregister:campaign:26V610000Wed, 23 Sep 2026 12:00:00 GMTNHTSA campaign 26V610000. NHTSA received the report on 23 Sep 2026. Manufacturer: Forest River, Inc. Units: 41. Defect, in the NHTSA record: "Forest River, Inc. (Forest River) is recalling certain 2026-2027 Dynamax Isata recreational vehicles. The bunk mat may not be properly aligned."https://recallregister.com/fda/ii/99058/recallregister:fda:device/99058Wed, 23 Sep 2026 12:00:00 GMTFDA event 99058, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: ICU Medical, Inc. Reason for recall, in the words of FDA: "Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out."https://recallregister.com/month/2026-09/#fda-99298recallregister:fda:device/99298Wed, 23 Sep 2026 12:00:00 GMTFDA event 99298, device. Class I. FDA report date: 23 Sep 2026. Reason for recall, in the words of FDA: "Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance."https://recallregister.com/fda/ii/99356/recallregister:fda:device/99356Wed, 23 Sep 2026 12:00:00 GMTFDA event 99356, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Nuclein LLC. Reason for recall, in the words of FDA: "Due to a software issue"https://recallregister.com/fda/ii/99452/recallregister:fda:device/99452Wed, 23 Sep 2026 12:00:00 GMTFDA event 99452, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Wilson-Cook Medical Inc. Reason for recall, in the words of FDA: "Due to issue with endoscope adherence and inability to spray powder. Firm will provide an updated Instruction for Use (IFU)."https://recallregister.com/fda/ii/99512/recallregister:fda:device/99512Wed, 23 Sep 2026 12:00:00 GMTFDA event 99512, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: restor3d Inc. Reason for recall, in the words of FDA: "Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation, reduced fixation or poor alignment of implants, implant loosening/migration, or need for revision surgery."https://recallregister.com/month/2026-09/#fda-99515recallregister:fda:device/99515Wed, 23 Sep 2026 12:00:00 GMTFDA event 99515, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: F & A Foundation. Reason for recall, in the words of FDA: "Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established."https://recallregister.com/fda/i/99534/recallregister:fda:device/99534Wed, 23 Sep 2026 12:00:00 GMTFDA event 99534, device. Class I. FDA report date: 23 Sep 2026. Recalling firm: Bard Access Systems, Inc. Reason for recall, in the words of FDA: "this is a downstream recall of class I recall RES 98777"https://recallregister.com/fda/i/99546/recallregister:fda:device/99546Wed, 23 Sep 2026 12:00:00 GMTFDA event 99546, device. Class I. FDA report date: 23 Sep 2026. Recalling firm: Nova Biomedical Corporation. Reason for recall, in the words of FDA: "A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode including patient identification (ID) barcodes and quality control (QC) solution ID barcodes when a new barcode is scanned, resulting in the prior barcode information remaining displayed on the screen for the current…"https://recallregister.com/fda/ii/99558/recallregister:fda:device/99558Wed, 23 Sep 2026 12:00:00 GMTFDA event 99558, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Howmedica Osteonics Corp. Reason for recall, in the words of FDA: "Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and…"https://recallregister.com/fda/ii/99566/recallregister:fda:device/99566Wed, 23 Sep 2026 12:00:00 GMTFDA event 99566, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Philips North America. Reason for recall, in the words of FDA: "Due to software malfunction, patient information system may freeze and become unresponsive."https://recallregister.com/fda/ii/99583/recallregister:fda:device/99583Wed, 23 Sep 2026 12:00:00 GMTFDA event 99583, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Medline Industries, LP. Reason for recall, in the words of FDA: "The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be assured. If a compromised pouch seal is not identified prior to use and the cannula is used, there is a potential risk of infection or other complications associated with the use of a non-sterile device, including hemolysis, foreign body…"https://recallregister.com/fda/ii/99593/recallregister:fda:device/99593Wed, 23 Sep 2026 12:00:00 GMTFDA event 99593, device. Class II. FDA report date: 23 Sep 2026. Reason for recall, in the words of FDA: "Retrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices."https://recallregister.com/fda/ii/99608/recallregister:fda:device/99608Wed, 23 Sep 2026 12:00:00 GMTFDA event 99608, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Happiest Baby, Inc. Reason for recall, in the words of FDA: "Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA."https://recallregister.com/fda/ii/99621/recallregister:fda:device/99621Wed, 23 Sep 2026 12:00:00 GMTFDA event 99621, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: NOXBOX LTD. Reason for recall, in the words of FDA: "Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation."https://recallregister.com/fda/ii/99628/recallregister:fda:device/99628Wed, 23 Sep 2026 12:00:00 GMTFDA event 99628, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Medical Action Industries, Inc. 306. Reason for recall, in the words of FDA: "Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's sterile barrier and if used may lead to localized skin or soft tissue infection."https://recallregister.com/fda/ii/99630/recallregister:fda:device/99630Wed, 23 Sep 2026 12:00:00 GMTFDA event 99630, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Boston Scientific Corporation. Reason for recall, in the words of FDA: "A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power adaptor may fail electrical safety testing during installation."https://recallregister.com/fda/ii/99634/recallregister:fda:device/99634Wed, 23 Sep 2026 12:00:00 GMTFDA event 99634, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Stryker Sustainability Solutions. Reason for recall, in the words of FDA: "Reusable access port system may crack or seperate during use."https://recallregister.com/fda/ii/99637/recallregister:fda:device/99637Wed, 23 Sep 2026 12:00:00 GMTFDA event 99637, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: GE Medical Systems Information Technologies Inc. Reason for recall, in the words of FDA: "Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events."https://recallregister.com/fda/ii/99648/recallregister:fda:device/99648Wed, 23 Sep 2026 12:00:00 GMTFDA event 99648, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: ICU Medical, Inc. Reason for recall, in the words of FDA: "Reservoirs may exhibit medication leakage at the joint between luer connector and tubing. Issue could result in delay or interruption of therapy, under delivery of medication, exposure to infectious or toxic agents, or air embolus."https://recallregister.com/fda/ii/99649/recallregister:fda:device/99649Wed, 23 Sep 2026 12:00:00 GMTFDA event 99649, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Datex-Ohmeda, Inc. Reason for recall, in the words of FDA: "Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling continued controlled or manual ventilation and initiates audible and visual alarms. When this issue occurs, anesthetic agent delivery will be interrupted and requires clinician…"https://recallregister.com/fda/ii/99661/recallregister:fda:device/99661Wed, 23 Sep 2026 12:00:00 GMTFDA event 99661, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: GE Healthcare. Reason for recall, in the words of FDA: "Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care."https://recallregister.com/month/2026-09/#fda-99664recallregister:fda:device/99664Wed, 23 Sep 2026 12:00:00 GMTFDA event 99664, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: PI CARDIA LTD. Reason for recall, in the words of FDA: "Transfemoral catheter, positing arm may detached due to weld issue."https://recallregister.com/fda/ii/99667/recallregister:fda:device/99667Wed, 23 Sep 2026 12:00:00 GMTFDA event 99667, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Medline Industries, LP. Reason for recall, in the words of FDA: "Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used."https://recallregister.com/fda/ii/99668/recallregister:fda:device/99668Wed, 23 Sep 2026 12:00:00 GMTFDA event 99668, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Maquet Cardiopulmonary Gmbh. Reason for recall, in the words of FDA: "The packaging may not consistently maintain sterile barrier integrity."https://recallregister.com/fda/i/99669/recallregister:fda:device/99669Wed, 23 Sep 2026 12:00:00 GMTFDA event 99669, device. Class I. FDA report date: 23 Sep 2026. Recalling firm: Medline Industries, LP. Reason for recall, in the words of FDA: "The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death."https://recallregister.com/fda/i/99671/recallregister:fda:device/99671Wed, 23 Sep 2026 12:00:00 GMTFDA event 99671, device. Class I. FDA report date: 23 Sep 2026. Recalling firm: Abiomed, Inc. Reason for recall, in the words of FDA: "The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly."https://recallregister.com/fda/i/99672/recallregister:fda:device/99672Wed, 23 Sep 2026 12:00:00 GMTFDA event 99672, device. Class I. FDA report date: 23 Sep 2026. Recalling firm: AVID Medical, Inc. Reason for recall, in the words of FDA: "Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides"https://recallregister.com/fda/ii/99677/recallregister:fda:device/99677Wed, 23 Sep 2026 12:00:00 GMTFDA event 99677, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Mirion Technologies (Capintec), Inc. Reason for recall, in the words of FDA: "Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from the ground."https://recallregister.com/month/2026-09/#fda-99685recallregister:fda:device/99685Wed, 23 Sep 2026 12:00:00 GMTFDA event 99685, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: WELL LEAD MEDICAL CO. LTD. Reason for recall, in the words of FDA: "The 6Fr suction catheter could not pass through the samples smoothly."https://recallregister.com/fda/ii/99698/recallregister:fda:device/99698Wed, 23 Sep 2026 12:00:00 GMTFDA event 99698, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Bayer Medical Care, Inc. Reason for recall, in the words of FDA: "Some devices may not have been properly sterilized due to a manufacturing sterilization issue."https://recallregister.com/fda/ii/99707/recallregister:fda:device/99707Wed, 23 Sep 2026 12:00:00 GMTFDA event 99707, device. Class II. FDA report date: 23 Sep 2026. Recalling firm: Straumann USA LLC. Reason for recall, in the words of FDA: "There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside."https://recallregister.com/month/2026-09/#fda-99720recallregister:fda:device/99720Wed, 23 Sep 2026 12:00:00 GMTFDA event 99720, device. Class II. FDA report date: 23 Sep 2026. Reason for recall, in the words of FDA: "When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead users to incorrectly omit the bolus during treatment and deliver the prescribed dose to the wrong tissue depth."https://recallregister.com/fda/i/99758/recallregister:fda:device/99758Wed, 23 Sep 2026 12:00:00 GMTFDA event 99758, device. Class I. FDA report date: 23 Sep 2026. Recalling firm: AVID Medical, Inc. Reason for recall, in the words of FDA: "Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical."https://recallregister.com/fda/ii/99654/recallregister:fda:drug/99654Wed, 23 Sep 2026 12:00:00 GMTFDA event 99654, drug. Class II. FDA report date: 23 Sep 2026. Recalling firm: Safecor Health, LLC. Reason for recall, in the words of FDA: "Failed Stability Specifications"https://recallregister.com/month/2026-09/#fda-99709recallregister:fda:drug/99709Wed, 23 Sep 2026 12:00:00 GMTFDA event 99709, drug. Class I. FDA report date: 23 Sep 2026. Recalling firm: VITRUVIAS THERAPEUTICS INC. Reason for recall, in the words of FDA: "Superpotent Drug"https://recallregister.com/month/2026-09/#fda-99794recallregister:fda:drug/99794Wed, 23 Sep 2026 12:00:00 GMTFDA event 99794, drug. Class II. FDA report date: 23 Sep 2026. Recalling firm: SUN PHARMA /TARO. Reason for recall, in the words of FDA: "Failed Content Uniformity Specifications. Out of Specification for Assay during analysis at the 24- month long term stability station, at (25°C,60%RH)."https://recallregister.com/month/2026-09/#fda-99806recallregister:fda:drug/99806Wed, 23 Sep 2026 12:00:00 GMTFDA event 99806, drug. Class II. FDA report date: 23 Sep 2026. Recalling firm: Inventia Healthcare Limited. Reason for recall, in the words of FDA: "Failed Dissolution Specifications"https://recallregister.com/fda/ii/99824/recallregister:fda:drug/99824Wed, 23 Sep 2026 12:00:00 GMTFDA event 99824, drug. Class II. FDA report date: 23 Sep 2026. Recalling firm: Pfizer. Reason for recall, in the words of FDA: "Lack of Assurance of Sterility"https://recallregister.com/fda/unclassified/99876/recallregister:fda:drug/99876Wed, 23 Sep 2026 12:00:00 GMTFDA event 99876, drug. Not yet classified. FDA report date: 23 Sep 2026. Recalling firm: SUN PHARMACEUTICAL INDUSTRIES INC. Reason for recall, in the words of FDA: "Failed Stability Specifications"https://recallregister.com/fda/ii/99572/recallregister:fda:food/99572Wed, 23 Sep 2026 12:00:00 GMTFDA event 99572, food. Class II. FDA report date: 23 Sep 2026. Recalling firm: Elegant Foods, LLC. Reason for recall, in the words of FDA: "Undeclared sulfites"https://recallregister.com/fda/i/99594/recallregister:fda:food/99594Wed, 23 Sep 2026 12:00:00 GMTFDA event 99594, food. Class I. FDA report date: 23 Sep 2026. Recalling firm: NatureBest Pre-Cut & Produce LLc. Reason for recall, in the words of FDA: "Jalapenos have the potential to be contaminated with Salmonella"https://recallregister.com/fda/i/99611/recallregister:fda:food/99611Wed, 23 Sep 2026 12:00:00 GMTFDA event 99611, food. Class I. FDA report date: 23 Sep 2026. Recalling firm: Taylor Fresh Foods Inc. Reason for recall, in the words of FDA: "Potential contamination with Salmonella."https://recallregister.com/fda/i/99737/recallregister:fda:food/99737Wed, 23 Sep 2026 12:00:00 GMTFDA event 99737, food. Class I. FDA report date: 23 Sep 2026. Recalling firm: Everything Sprouts, LLC. Reason for recall, in the words of FDA: "Sprouts may be contaminated with STEC E. coli and/or Salmonella."https://recallregister.com/month/2026-09/#fda-99744recallregister:fda:food/99744Wed, 23 Sep 2026 12:00:00 GMTFDA event 99744, food. Class II. FDA report date: 23 Sep 2026. Recalling firm: Buckhead Meat Company D.B.A. Trinity Seafood. Reason for recall, in the words of FDA: "The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin."https://recallregister.com/month/2026-09/#fda-99755recallregister:fda:food/99755Wed, 23 Sep 2026 12:00:00 GMTFDA event 99755, food. Class II. FDA report date: 23 Sep 2026. Recalling firm: Quality Dairy Farms Inc. Reason for recall, in the words of FDA: "Undeclared peanuts"https://recallregister.com/month/2026-09/#fda-99780recallregister:fda:food/99780Wed, 23 Sep 2026 12:00:00 GMTFDA event 99780, food. Class II. FDA report date: 23 Sep 2026. Recalling firm: Panorama Produce Sales Inc. Reason for recall, in the words of FDA: "Product may be contaminated with Salmonella"https://recallregister.com/month/2026-09/#fda-99803recallregister:fda:food/99803Wed, 23 Sep 2026 12:00:00 GMTFDA event 99803, food. Class II. FDA report date: 23 Sep 2026. Recalling firm: Best Friends Bakery, LLC. Reason for recall, in the words of FDA: "Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product."https://recallregister.com/fda/iii/99815/recallregister:fda:food/99815Wed, 23 Sep 2026 12:00:00 GMTFDA event 99815, food. Class III. FDA report date: 23 Sep 2026. Recalling firm: Tiffany Food Corp. Reason for recall, in the words of FDA: "Unapproved dye Ponceau 4R"https://recallregister.com/month/2026-09/#fda-99830recallregister:fda:food/99830Wed, 23 Sep 2026 12:00:00 GMTFDA event 99830, food. Class I. FDA report date: 23 Sep 2026. Recalling firm: FOODS ALIVE INC. Reason for recall, in the words of FDA: "Potential Salmonella contamination"https://recallregister.com/month/2026-09/#fda-99831recallregister:fda:food/99831Wed, 23 Sep 2026 12:00:00 GMTFDA event 99831, food. Class I. FDA report date: 23 Sep 2026. Recalling firm: Frutas y Hortalizas del Sur S.A. Reason for recall, in the words of FDA: "Potential E. coli O145:H28 Contamination"https://recallregister.com/month/2026-09/#fda-99841recallregister:fda:food/99841Wed, 23 Sep 2026 12:00:00 GMTFDA event 99841, food. Class I. FDA report date: 23 Sep 2026. Recalling firm: Optimus Inc. d/b/a/ Markys Caviar. Reason for recall, in the words of FDA: "The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes."https://recallregister.com/fda/unclassified/99869/recallregister:fda:food/99869Wed, 23 Sep 2026 12:00:00 GMTFDA event 99869, food. Not yet classified. FDA report date: 23 Sep 2026. Recalling firm: KRAFT HEINZ FOODS COMPANY. Reason for recall, in the words of FDA: "undeclared ingredients including but not limited to mustard"https://recallregister.com/equipment/other/#26E065000recallregister:campaign:26E065000Tue, 22 Sep 2026 12:00:00 GMTNHTSA campaign 26E065000. NHTSA received the report on 22 Sep 2026. Manufacturer: Ford Motor Company. Units: 46. Defect, in the NHTSA record: "Ford Motor Company (Ford) is recalling certain 10.1-inch center stack screens installed in 2024-2026 Ranger vehicles during service. The screen may lose power and fail to display the rearview camera image. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility.""https://recallregister.com/vehicle/nova-bus/lfs/2025/#26V604000recallregister:campaign:26V604000Tue, 22 Sep 2026 12:00:00 GMTNHTSA campaign 26V604000. NHTSA received the report on 22 Sep 2026. Manufacturer: Nova Bus (US) Inc. Units: 5. Defect, in the NHTSA record: "Nova Bus (US) Inc. (Nova Bus) is recalling certain 2024-2025 LFS transit buses. The emergency brake valve may have been improperly tightened. A loose connection may cause an air leak and the unintentional activation of the parking brake."https://recallregister.com/vehicle/ford/ranger/2026/#26V605000recallregister:campaign:26V605000Tue, 22 Sep 2026 12:00:00 GMTNHTSA campaign 26V605000. NHTSA received the report on 22 Sep 2026. Manufacturer: Ford Motor Company. Units: 11,405. Defect, in the NHTSA record: "Ford Motor Company (Ford) is recalling certain 2026 Ranger vehicles equipped with a 10.1-inch center stack screen. The screen may lose power and fail to display the rearview camera image. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility.""https://recallregister.com/vehicle/ford/f-450-sd/2026/#26V606000recallregister:campaign:26V606000Tue, 22 Sep 2026 12:00:00 GMTNHTSA campaign 26V606000. NHTSA received the report on 22 Sep 2026. Manufacturer: Ford Motor Company. Units: 41,748. Defect, in the NHTSA record: "Ford Motor Company (Ford) is recalling certain 2025-2027 Expedition, 2026 F-250 SD, F-350 SD, F-450 SD, and F-550 SD vehicles. The headlight assemblies may contain a contaminated LED chip, which can result in a loss of daytime running lights, parking lights, high beams or low beams. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment.""https://recallregister.com/vehicle/dynamax/grand-sport-gt/2027/#26V603000recallregister:campaign:26V603000Mon, 21 Sep 2026 12:00:00 GMTNHTSA campaign 26V603000. NHTSA received the report on 21 Sep 2026. Manufacturer: Forest River, Inc. Units: 16. Defect, in the NHTSA record: "Forest River, Inc (Forest River) is recalling certain 2026-2027 Dynamax Grand Sport GT recreational vehicles. The engine pre-heat pump may have been improperly installed, causing the coolant hose to fail."https://recallregister.com/vehicle/volvo-bus/9700/2025/#26V600000recallregister:campaign:26V600000Fri, 18 Sep 2026 12:00:00 GMTNHTSA campaign 26V600000. NHTSA received the report on 18 Sep 2026. Manufacturer: Volvo Bus Corporation. Units: 1,236. Defect, in the NHTSA record: "Volvo Bus Corporation (Volvo Bus) is recalling certain 2009-2025 Volvo 9700 buses. The emergency exit label on the entrance door is missing the exit operating instructions. As such, these vehicles fail to conform to Federal Motor Vehicle Safety Standard (FMVSS) number 217, "Bus Emergency Exits and Window Retention and Release.""https://recallregister.com/make/winnebago/#26V601000recallregister:campaign:26V601000Fri, 18 Sep 2026 12:00:00 GMTNHTSA campaign 26V601000. NHTSA received the report on 18 Sep 2026. Manufacturer: Winnebago Industries, Inc. Units: 56. Defect, in the NHTSA record: "Winnebago Industries, Inc. (Winnebago) is recalling certain 2027 Arka recreational vehicles. The rear Gross Axle Weight Rating (GAWR) and cold tire inflation listed on the federal placard is incorrect. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims - Other than Passenger Cars.""https://recallregister.com/vehicle/fleetwood/palisade/2026/#26V602000recallregister:campaign:26V602000Fri, 18 Sep 2026 12:00:00 GMTNHTSA campaign 26V602000. NHTSA received the report on 18 Sep 2026. Manufacturer: REV Recreation Group. Units: 47. Defect, in the NHTSA record: "REV Recreation Group (REV) is recalling certain 2025-2026 American Coach American Dream, 2026-2027 Fleetwood Discovery LXE, 2026 Fleetwood Palisade, and Holiday Rambler Armada recreational vehicles. The RoadWatch Safety System may have been programmed with the incorrect vehicle parameters."https://recallregister.com/vehicle/lexus/tx-hybrid/2026/#26V598000recallregister:campaign:26V598000Thu, 17 Sep 2026 12:00:00 GMTNHTSA campaign 26V598000. NHTSA received the report on 17 Sep 2026. Manufacturer: Toyota Motor Engineering & Manufacturing. Units: 617. Defect, in the NHTSA record: "Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2026 Lexus TX350, RX350 Hybrid, RX350, RX500 Hybrid, TX500 Hybrid, Toyota Grand Highlander, and Grand Highlander Hybrid vehicles. Due to a manufacturing error, the front steering knuckles may crack and break, which can result in a loss of vehicle steering control."https://recallregister.com/vehicle/land-rover/range-rover-sport/2024/#26V599000recallregister:campaign:26V599000Thu, 17 Sep 2026 12:00:00 GMTNHTSA campaign 26V599000. NHTSA received the report on 17 Sep 2026. Manufacturer: Jaguar Land Rover North America, LLC. Units: 23,677. Defect, in the NHTSA record: "Jaguar Land Rover North America, LLC (Land Rover) is recalling certain 2019-2024 Land Rover Range Rover Sport, 2020-2024 Land Rover Range Rover Evoque, Land Rover Range Rover, Land Rover Discovery Sport, Land Rover Defender, 2021-2024 Land Rover Range Rover Velar, Jaguar E-Pace, F-Pace, and Land Rover Discovery vehicles. The DC-DC converter may malfunction due to an electrical overload that can occur during high power demand. Additionally, a software error can cause the DC-DC converter to stop functioning at vehicle start-up under certain circumstances. Failure of the DC-DC converter will result in the loss of 12-Volt system charging and can lead to complete loss of drive power and…"https://recallregister.com/product/10974-colerinsec-recalls-jerify-magnetic-stick-figure-toy-sets-due-to-risk-o/recallregister:product:10974Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26774. Recall date: 17 Sep 2026. Firm: Hefei Hanchan Network Technology Co., Ltd., dba Colerinsec. Units: 38,507. Hazard, in the words of CPSC: "The magnetic humanoid toy Sets violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death."https://recallregister.com/product/10975-jkmax-recalls-heated-blankets-and-heating-pads-due-to-fire-and-burn-ha/recallregister:product:10975Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26778. Recall date: 17 Sep 2026. Firm: Jiande Pengshuai Trading. Units: 195,000. Hazard, in the words of CPSC: "The internal wire heating elements of the blankets and pads can overheat, posing fire and burn hazards to consumers."https://recallregister.com/product/10976-melissa-doug-recalls-fire-truck-activity-board-toys-due-to-risk-of-ser/recallregister:product:10976Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26780. Recall date: 17 Sep 2026. Units: 84,000. Hazard, in the words of CPSC: "The fire hose port can come loose and detach, posing a risk of serious injury from choking hazard."https://recallregister.com/product/10977-shein-distribution-corporation-recalls-pull-and-chew-montessori-teethi/recallregister:product:10977Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26782. Recall date: 17 Sep 2026. Firm: SHEIN Distribution. Units: 644. Hazard, in the words of CPSC: "The recalled teething toys violate the mandatory safety standard for toys because the silicone strings are smaller and longer than permitted. The silicone strings can reach the back of the throat and become lodged, posing a risk of respiratory distress and a deadly choking hazard."https://recallregister.com/product/10978-tongyang-cycling-recalls-basecamp-bicycle-helmets-due-to-risk-of-serio/recallregister:product:10978Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26785. Recall date: 17 Sep 2026. Firm: HK Tongyang Technology Co., Ltd., dba Tongyang Cycling. Units: 315. Hazard, in the words of CPSC: "The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional stability and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury. In addition, the helmets have a button cell battery that does not bear the warning labels required by Reese's Law. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death."https://recallregister.com/product/10979-sauna360-expands-recall-of-tylo-halmstad-and-kiruna-hybrid-saunas-due/recallregister:product:10979Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26783. Recall date: 17 Sep 2026. Firm: SFactor. Units: 6,000. Hazard, in the words of CPSC: "The saunas contain a bench that can collapse, posing a fall hazard to consumers. The previous recall repair was ineffective; a new repair is now being offered."https://recallregister.com/product/10980-toyworld168-recalls-rainbow-mystery-squishy-bun-toys-due-to-risk-of-se/recallregister:product:10980Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26786. Recall date: 17 Sep 2026. Firm: Toyworld168. Units: 276. Hazard, in the words of CPSC: "The squishy bun toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly ingestion hazard. If a water bead is ingested, it can pose ingestion, choking and intestinal obstruction hazards inside a child's body, resulting in severe discomfort, vomiting, dehydration and a risk of death to a child."https://recallregister.com/product/10981-regfear-recalls-bedspick-mattresses-due-to-risk-of-serious-injury-or-d/recallregister:product:10981Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26781. Recall date: 17 Sep 2026. Firm: Regfear. Units: 818. Hazard, in the words of CPSC: "The mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire."https://recallregister.com/product/10982-esjay-us-recalls-toddler-busy-board-montessori-toys-due-to-risk-of-ser/recallregister:product:10982Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26775. Recall date: 17 Sep 2026. Firm: Shenzhen Yishijie Technology Co., Ltd., dba Esjay US. Units: 276,000. Hazard, in the words of CPSC: "The recalled toy violates the small parts ban because the product is for children under three years of age and the red knobs can detach, posing a deadly choking hazard."https://recallregister.com/product/10983-lanchez-pressure-washers-recalled-due-to-serious-risk-of-injury-or-dea/recallregister:product:10983Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26779. Recall date: 17 Sep 2026. Firm: Ningbo Lanchez E-Commerce Co., Ltd. of China. Units: 329. Hazard, in the words of CPSC: "The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, which may encourage use of an extension cord, posing serious risks of injury or death from shock and electrocution hazards."https://recallregister.com/product/10984-sauna360-recalls-infrared-saunas-hybrid-infrared-saunas-and-infrared-k/recallregister:product:10984Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26784. Recall date: 17 Sep 2026. Firm: Sauna360. Units: 41,580. Hazard, in the words of CPSC: "The infrared panels in the saunas and kits can short circuit, causing them to overheat, posing a risk of serious injury from fire and burn hazards."https://recallregister.com/product/10985-friedrich-air-conditioning-recalls-kuhl-window-air-conditioners-due-to/recallregister:product:10985Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26776. Recall date: 17 Sep 2026. Firm: Friedrich Air Conditioning. Units: 2,000. Hazard, in the words of CPSC: "The control board inside the motor of the recalled air conditioners can fail, posing a risk of serious injury or death from fire and burn hazards."https://recallregister.com/product/10986-char-broil-recalls-bistro-pro-electric-grills-due-to-risk-of-electric/recallregister:product:10986Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26773. Recall date: 17 Sep 2026. Firm: Char-Broil. Units: 10,605. Hazard, in the words of CPSC: "The grounding wire for the grill's heating element can disconnect and lose fault protection, posing an electric shock hazard."https://recallregister.com/product/10987-hayward-industries-recalls-universal-pool-heaters-due-to-risk-of-serio/recallregister:product:10987Thu, 17 Sep 2026 12:00:00 GMTCPSC recall 26777. Recall date: 17 Sep 2026. Firm: Hayward Industries. Units: 4,600. Hazard, in the words of CPSC: "During operation, the heaters can produce high levels of carbon monoxide (CO), posing a risk of serious injury or death from carbon monoxide poisoning."https://recallregister.com/month/2026-09/#26V596000recallregister:campaign:26V596000Wed, 16 Sep 2026 12:00:00 GMTNHTSA campaign 26V596000. NHTSA received the report on 16 Sep 2026. Manufacturer: Rewaco Spezialfahrzeuge GmbH. Units: 106. Defect, in the NHTSA record: "Rewaco Spezialfahrzeuge GmbH (Rewaco) is recalling certain 2024 RF1 ST-3, 2024-2025 PUR3 GT, 2024-2026 RF1 ST-3 Touring, RF1 GT Touring, and PUR3 GT Touring three-wheeled motorcycles. The connection between the piston rod and rod end in the rear shock absorbers may loosen, resulting in a loss of vehicle control."https://recallregister.com/vehicle/rivian/r1t/2026/#26V597000recallregister:campaign:26V597000Wed, 16 Sep 2026 12:00:00 GMTNHTSA campaign 26V597000. NHTSA received the report on 16 Sep 2026. Manufacturer: Rivian Automotive, LLC. Units: 98,828. Defect, in the NHTSA record: "Rivian Automotive, LLC (Rivian) is recalling certain 2022-2027 R1S, 2022-2026 R1T, and 2027 R2 vehicles. The rearview camera image may be obstructed by a notification when in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 111, "Rear Visibility.""https://recallregister.com/fda/ii/98840/recallregister:fda:device/98840Wed, 16 Sep 2026 12:00:00 GMTFDA event 98840, device. Class II. FDA report date: 16 Sep 2026. Recalling firm: C.R. Bard Inc. Reason for recall, in the words of FDA: "Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays."https://recallregister.com/fda/ii/99525/recallregister:fda:device/99525Wed, 16 Sep 2026 12:00:00 GMTFDA event 99525, device. Class II. FDA report date: 16 Sep 2026. Recalling firm: AVID Medical, Inc. Reason for recall, in the words of FDA: "Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area."https://recallregister.com/fda/ii/99568/recallregister:fda:device/99568Wed, 16 Sep 2026 12:00:00 GMTFDA event 99568, device. Class II. FDA report date: 16 Sep 2026. Recalling firm: HeartSine Technologies Ltd. Reason for recall, in the words of FDA: "Due to a damaged (over stretched) membrane tail that causes an intermittent fault."https://recallregister.com/fda/ii/99573/recallregister:fda:device/99573Wed, 16 Sep 2026 12:00:00 GMTFDA event 99573, device. Class II. FDA report date: 16 Sep 2026. Recalling firm: Nipro Renal Soultions USA, Corporation. Reason for recall, in the words of FDA: "Hemodialysis concentrates contain high endotoxin levels"https://recallregister.com/fda/ii/99601/recallregister:fda:device/99601Wed, 16 Sep 2026 12:00:00 GMTFDA event 99601, device. Class II. FDA report date: 16 Sep 2026. Recalling firm: Lutronic Corporation. Reason for recall, in the words of FDA: "Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn."https://recallregister.com/fda/i/99613/recallregister:fda:device/99613Wed, 16 Sep 2026 12:00:00 GMTFDA event 99613, device. Class I. FDA report date: 16 Sep 2026. Recalling firm: Medical Action Industries, Inc. 306. Reason for recall, in the words of FDA: "Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility."https://recallregister.com/fda/i/99626/recallregister:fda:device/99626Wed, 16 Sep 2026 12:00:00 GMTFDA event 99626, device. Class I. FDA report date: 16 Sep 2026. Recalling firm: Given Imaging Ltd. Reason for recall, in the words of FDA: "Capsule may fail to attach to the esophagus or detach from the delivery device. Risks include patient aspiration/inhalation, perforation of esophagus, obstruction of the airway, hemorrhage/blood loss/bleeding, laceration of the esophagus, a delay in diagnosis, and foreign bodies remaining in the patient."https://recallregister.com/fda/ii/99658/recallregister:fda:device/99658Wed, 16 Sep 2026 12:00:00 GMTFDA event 99658, device. Class II. FDA report date: 16 Sep 2026. Recalling firm: Windstone Medical Packaging, Inc. Reason for recall, in the words of FDA: "The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the infusion port during manipulation."https://recallregister.com/fda/ii/99680/recallregister:fda:device/99680Wed, 16 Sep 2026 12:00:00 GMTFDA event 99680, device. Class II. FDA report date: 16 Sep 2026. Recalling firm: Atrium Medical Corporation. Reason for recall, in the words of FDA: "An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters."https://recallregister.com/fda/i/99670/recallregister:fda:drug/99670Wed, 16 Sep 2026 12:00:00 GMTFDA event 99670, drug. Class I. FDA report date: 16 Sep 2026. Recalling firm: American Regent, Inc. Reason for recall, in the words of FDA: "Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass and broken and leaking vials."https://recallregister.com/fda/i/99679/recallregister:fda:drug/99679Wed, 16 Sep 2026 12:00:00 GMTFDA event 99679, drug. Class I. FDA report date: 16 Sep 2026. Recalling firm: Baxter Healthcare Corporation. Reason for recall, in the words of FDA: "Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution."https://recallregister.com/fda/i/99703/recallregister:fda:drug/99703Wed, 16 Sep 2026 12:00:00 GMTFDA event 99703, drug. Class I. FDA report date: 16 Sep 2026. Recalling firm: B BRAUN MEDICAL INC. Reason for recall, in the words of FDA: "Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene"https://recallregister.com/fda/iii/99733/recallregister:fda:drug/99733Wed, 16 Sep 2026 12:00:00 GMTFDA event 99733, drug. Class III. FDA report date: 16 Sep 2026. Recalling firm: Ajanta Pharma USA Inc. Reason for recall, in the words of FDA: "Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result: 1.1 percent. Spec: 1.0 percent."https://recallregister.com/month/2026-09/#fda-99756recallregister:fda:drug/99756Wed, 16 Sep 2026 12:00:00 GMTFDA event 99756, drug. Class III. FDA report date: 16 Sep 2026. Recalling firm: ImprimisRx NJ LLC. Reason for recall, in the words of FDA: "Subpotent Drug"https://recallregister.com/fda/ii/99837/recallregister:fda:drug/99837Wed, 16 Sep 2026 12:00:00 GMTFDA event 99837, drug. Class II. FDA report date: 16 Sep 2026. Recalling firm: OurPharma LLC. Reason for recall, in the words of FDA: "Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry (12/09/2026)."https://recallregister.com/month/2026-09/#fda-99636recallregister:fda:food/99636Wed, 16 Sep 2026 12:00:00 GMTFDA event 99636, food. Class I. FDA report date: 16 Sep 2026. Recalling firm: EXOTIQUE FOODS CANADA. Reason for recall, in the words of FDA: "Undeclared Wheat."https://recallregister.com/month/2026-09/#fda-99675recallregister:fda:food/99675Wed, 16 Sep 2026 12:00:00 GMTFDA event 99675, food. Class II. FDA report date: 16 Sep 2026. Recalling firm: L-Nutra Inc. Reason for recall, in the words of FDA: "Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio."https://recallregister.com/month/2026-09/#fda-99682recallregister:fda:food/99682Wed, 16 Sep 2026 12:00:00 GMTFDA event 99682, food. Class II. FDA report date: 16 Sep 2026. Recalling firm: Ferrero USA. Reason for recall, in the words of FDA: "Undeclared milk and pecans"https://recallregister.com/month/2026-09/#fda-99684recallregister:fda:food/99684Wed, 16 Sep 2026 12:00:00 GMTFDA event 99684, food. Class I. FDA report date: 16 Sep 2026. Recalling firm: EURO FOODS GROUP USA NJ INC. Reason for recall, in the words of FDA: "The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying."https://recallregister.com/month/2026-09/#fda-99822recallregister:fda:food/99822Wed, 16 Sep 2026 12:00:00 GMTFDA event 99822, food. Class I. FDA report date: 16 Sep 2026. Recalling firm: International Sprout Holdings, Inc. Reason for recall, in the words of FDA: "Potential E. coli and Salmonella contamination"