Recall Register: FDA Class I recalls

Recall Register: FDA Class I recallshttps://recallregister.com/New FDA enforcement events that FDA put in Class I.enWed, 23 Sep 2026 12:00:00 GMTBD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris… recall, Class I (FDA event 99298)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."Power-Trialysis Short-Term Straight Dialysis Catheter recall: Bard Access Systems, Inc., Class I (FDA event 99534)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"StatStrip Glucose Hospital Meter System recall: Nova Biomedical Corporation, Class I (FDA event 99546)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…"Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET recall: Medline Industries, LP, Class I (FDA event 99669)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."Automated Impella Controller (AIC) with the below product descriptions and… recall: Abiomed, Inc., Class I (FDA event 99671)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."Halyard IV START KIT NON-STERILE REF: KRIV26-02 recall: AVID Medical, Inc., Class I (FDA event 99672)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"Haylard 18G SINGLE SHOT EPI TRAY recall: AVID Medical, Inc., Class I (FDA event 99758)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."Thyroid Tablets recall: VITRUVIAS THERAPEUTICS INC, Class I (FDA event 99709)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"PICO DE GALLO-MILD-4oz PICO DE GALLO-MILD-6/14oz PICO DE GALLO-4/5# PICO DE… recall: NatureBest Pre-Cut & Produce LLc, Class I (FDA event 99594)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"Diced Jalapenos recall: Taylor Fresh Foods Inc, Class I (FDA event 99611)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."Everything Sprouts and Calco branded Alfalfa Sprouts recall: Everything Sprouts, LLC, Class I (FDA event 99737)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."Foods Alive organic moringa leaf powder recall: FOODS ALIVE INC., Class I (FDA event 99830)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"Organic Triple Berry Blend Strawberries recall: Frutas y Hortalizas del Sur S.A., Class I (FDA event 99831)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"Mon Sire Brie, soft-ripened French cheese recall: Optimus Inc. d/b/a/ Markys Caviar, Class I (FDA event 99841)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."Kit: Epidural/Pain TQC 20/Cs recall: Medical Action Industries, Inc. 306, Class I (FDA event 99613)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."Bravo CF capsule delivery device recall: Given Imaging Ltd., Class I (FDA event 99626)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."Epinephrine Injection recall: American Regent, Inc., Class I (FDA event 99670)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."Dextrose Injection recall: Baxter Healthcare Corporation, Class I (FDA event 99679)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."0.9% Sodium Chloride Injection recall: B BRAUN MEDICAL INC, Class I (FDA event 99703)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"Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower recall: EXOTIQUE FOODS CANADA, Class I (FDA event 99636)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."Crown Farms Dried Suri Cut recall: EURO FOODS GROUP USA NJ INC, Class I (FDA event 99684)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."Alfalfa, Net Weight 50 lbs recall: International Sprout Holdings, Inc, Class I (FDA event 99822)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"Glutathione 200 mg/mL recall: OPTIMAL BALANCE PHARMACY, Class I (FDA event 99662)https://recallregister.com/month/2026-09/#fda-99662recallregister:fda:drug/99662Wed, 09 Sep 2026 12:00:00 GMTFDA event 99662, drug. Class I. FDA report date: 9 Sep 2026. Recalling firm: OPTIMAL BALANCE PHARMACY. Reason for recall, in the words of FDA: "Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin."0.9% Sodium Chloride Injection USP 500 mL recall: Baxter Healthcare Corporation, Class I (FDA event 99678)https://recallregister.com/fda/i/99678/recallregister:fda:drug/99678Wed, 09 Sep 2026 12:00:00 GMTFDA event 99678, drug. Class I. FDA report date: 9 Sep 2026. Recalling firm: Baxter Healthcare Corporation. Reason for recall, in the words of FDA: "Presence of particulate matter: Particulates identified as fiberglass"OLA-OLA Pounded Yam (Iyan) IYANINSTANT recall: Fayus Inc., Class I (FDA event 99368)https://recallregister.com/month/2026-09/#fda-99368recallregister:fda:food/99368Wed, 09 Sep 2026 12:00:00 GMTFDA event 99368, food. Class I. FDA report date: 9 Sep 2026. Recalling firm: Fayus Inc. Reason for recall, in the words of FDA: "Undeclared milk."Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round plastic container recall: Ron's Home Style Foods, Inc., Class I (FDA event 99587)https://recallregister.com/fda/i/99587/recallregister:fda:food/99587Wed, 09 Sep 2026 12:00:00 GMTFDA event 99587, food. Class I. FDA report date: 9 Sep 2026. Recalling firm: Ron's Home Style Foods, Inc. Reason for recall, in the words of FDA: "Products were manufactured with jalapenos that have the potential to be contaminated with Salmonella"Frankie's Organic Plant-Based Puffs Vegan Cheddar recall: Marina Del Rey Foods inc., Class I (FDA event 99615)https://recallregister.com/month/2026-09/#fda-99615recallregister:fda:food/99615Wed, 09 Sep 2026 12:00:00 GMTFDA event 99615, food. Class I. FDA report date: 9 Sep 2026. Recalling firm: Marina Del Rey Foods inc. Reason for recall, in the words of FDA: "Product tested positive for undeclared milk."Organic Cheddar Type Seasoning recall: Savor Seasonings LLC, Class I (FDA event 99644)https://recallregister.com/month/2026-09/#fda-99644recallregister:fda:food/99644Wed, 09 Sep 2026 12:00:00 GMTFDA event 99644, food. Class I. FDA report date: 9 Sep 2026. Recalling firm: Savor Seasonings LLC. Reason for recall, in the words of FDA: "Product tested positive for undeclared milk allergen."THE HAMPTON GROCER brand recall: THE HAMPTON GROCER, Class I (FDA event 99656)https://recallregister.com/month/2026-09/#fda-99656recallregister:fda:food/99656Wed, 09 Sep 2026 12:00:00 GMTFDA event 99656, food. Class I. FDA report date: 9 Sep 2026. Recalling firm: THE HAMPTON GROCER. Reason for recall, in the words of FDA: "Product may be contaminated with Salmonella."Tyenne (tocilizumab-aazg) Injection recall: Fresenius Kabi USA, LLC, Class I (FDA event 99603)https://recallregister.com/fda/i/99603/recallregister:fda:drug/99603Wed, 02 Sep 2026 12:00:00 GMTFDA event 99603, drug. Class I. FDA report date: 2 Sep 2026. Recalling firm: Fresenius Kabi USA, LLC. Reason for recall, in the words of FDA: "Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles."Lactated Ringer's Injection USP recall: B BRAUN MEDICAL INC, Class I (FDA event 99633)https://recallregister.com/fda/i/99633/recallregister:fda:drug/99633Wed, 02 Sep 2026 12:00:00 GMTFDA event 99633, drug. Class I. FDA report date: 2 Sep 2026. Recalling firm: B BRAUN MEDICAL INC. Reason for recall, in the words of FDA: "Presence of Particulate matter."Addall XR Shot 1 single bottle recall: ZMB Enterprises, Class I (FDA event 98691)https://recallregister.com/month/2026-09/#fda-98691recallregister:fda:food/98691Wed, 02 Sep 2026 12:00:00 GMTFDA event 98691, food. Class I. FDA report date: 2 Sep 2026. Recalling firm: ZMB Enterprises. Reason for recall, in the words of FDA: "The product contains 1,4-DMAA, Phenylethylamine and Phenibut."Glutinous Rice Balls with Black Sesame Filling NET WT recall, Class I (FDA event 99424)https://recallregister.com/fda/i/99424/recallregister:fda:food/99424Wed, 02 Sep 2026 12:00:00 GMTFDA event 99424, food. Class I. FDA report date: 2 Sep 2026. Reason for recall, in the words of FDA: "Undeclared peanuts."bettergoods brand Pistachio Nut Butter recall: Botticelli Foods, LLC, Class I (FDA event 99538)https://recallregister.com/month/2026-09/#fda-99538recallregister:fda:food/99538Wed, 02 Sep 2026 12:00:00 GMTFDA event 99538, food. Class I. FDA report date: 2 Sep 2026. Recalling firm: Botticelli Foods, LLC. Reason for recall, in the words of FDA: "Product may be contaminated with Salmonella."Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base recall: H & U Inc. dba Sun Noodle, Class I (FDA event 99571)https://recallregister.com/month/2026-09/#fda-99571recallregister:fda:food/99571Wed, 02 Sep 2026 12:00:00 GMTFDA event 99571, food. Class I. FDA report date: 2 Sep 2026. Recalling firm: H & U Inc. dba Sun Noodle. Reason for recall, in the words of FDA: "Soba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into Sura Tanmen Hot and Sour Flavor ramen noodle package kit, but fish species are not declared on finished product label."Jalapeno Ranch, packed in 16 oz recall: Jaime's Foods ATX, LLC, Class I (FDA event 99575)https://recallregister.com/month/2026-09/#fda-99575recallregister:fda:food/99575Wed, 02 Sep 2026 12:00:00 GMTFDA event 99575, food. Class I. FDA report date: 2 Sep 2026. Recalling firm: Jaime's Foods ATX, LLC. Reason for recall, in the words of FDA: "Undeclared Egg Allergen"Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB recall: Sirna and Sons Produce, Inc, Class I (FDA event 99695)https://recallregister.com/month/2026-09/#fda-99695recallregister:fda:food/99695Wed, 02 Sep 2026 12:00:00 GMTFDA event 99695, food. Class I. FDA report date: 2 Sep 2026. Recalling firm: Sirna and Sons Produce, Inc. Reason for recall, in the words of FDA: "Potential Salmonella Javiana contamination"BMC/REACTHEALTH Luna G3 APAP REF LG 3600 recall: BMC Medical Co., Ltd., Class I (FDA event 99445)https://recallregister.com/month/2026-08/#fda-99445recallregister:fda:device/99445Wed, 26 Aug 2026 12:00:00 GMTFDA event 99445, device. Class I. FDA report date: 26 Aug 2026. Recalling firm: BMC Medical Co., Ltd. Reason for recall, in the words of FDA: "Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse"Boston Scientific ENROUTE Transcarotid Neuroprotection System recall: Boston Scientific Corporation, Class I (FDA event 99454)https://recallregister.com/fda/i/99454/recallregister:fda:device/99454Wed, 26 Aug 2026 12:00:00 GMTFDA event 99454, device. Class I. FDA report date: 26 Aug 2026. Recalling firm: Boston Scientific Corporation. Reason for recall, in the words of FDA: "Potential for arterial sheath tip separation or partial tip separation during use."BD Needle Kit for Powered Driver 15mm x 15Ga recall: Bard Access Systems, Inc., Class I (FDA event 99484)https://recallregister.com/fda/i/99484/recallregister:fda:device/99484Wed, 26 Aug 2026 12:00:00 GMTFDA event 99484, device. Class I. FDA report date: 26 Aug 2026. Recalling firm: Bard Access Systems, Inc. Reason for recall, in the words of FDA: "After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove obturator, due to it locking to the needle hub, due to out-of-tolerance dimensions and IFU unclarity, which may result in new needle placement, which may result in delayed therapy"Nitroglycerin injection recall: American Regent, Inc., Class I (FDA event 99503)https://recallregister.com/fda/i/99503/recallregister:fda:drug/99503Wed, 26 Aug 2026 12:00:00 GMTFDA event 99503, drug. Class I. FDA report date: 26 Aug 2026. Recalling firm: American Regent, Inc. Reason for recall, in the words of FDA: "Presence of Particulate Matter: Product contaminated with particulate matter identified as glass and/or paraformaldehyde"Morphine Sulfate Injection recall: Fresenius Kabi USA, LLC, Class I (FDA event 99533)https://recallregister.com/fda/i/99533/recallregister:fda:drug/99533Wed, 26 Aug 2026 12:00:00 GMTFDA event 99533, drug. Class I. FDA report date: 26 Aug 2026. Recalling firm: Fresenius Kabi USA, LLC. Reason for recall, in the words of FDA: "Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL."Organic Whole Blueberries recall: Publix Super Markets, Inc., Class I (FDA event 99542)https://recallregister.com/fda/i/99542/recallregister:fda:food/99542Wed, 26 Aug 2026 12:00:00 GMTFDA event 99542, food. Class I. FDA report date: 26 Aug 2026. Recalling firm: Publix Super Markets, Inc. Reason for recall, in the words of FDA: "Due to potential E. coli O145:H28 contamination"Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging recall: Coast Citrus Distributors, Class I (FDA event 99569)https://recallregister.com/month/2026-08/#fda-99569recallregister:fda:food/99569Wed, 26 Aug 2026 12:00:00 GMTFDA event 99569, food. Class I. FDA report date: 26 Aug 2026. Recalling firm: Coast Citrus Distributors. Reason for recall, in the words of FDA: "Potential Salmonella Javiana contamination"VITASIA ASIAN STYLE WOK SPICE MIX NET WT 1.58 OZ (45g) UPC 4 335619 355491… recall: Lidl US TRADING, Class I (FDA event 99618)https://recallregister.com/fda/i/99618/recallregister:fda:food/99618Wed, 26 Aug 2026 12:00:00 GMTFDA event 99618, food. Class I. FDA report date: 26 Aug 2026. Recalling firm: Lidl US TRADING. Reason for recall, in the words of FDA: "Salmonella. The firm received a positive test result of Salmonella in the product."Dairyland Produce recall: Dairyland Produce, LLC, Class I (FDA event 99635)https://recallregister.com/month/2026-08/#fda-99635recallregister:fda:food/99635Wed, 26 Aug 2026 12:00:00 GMTFDA event 99635, food. Class I. FDA report date: 26 Aug 2026. Recalling firm: Dairyland Produce, LLC. Reason for recall, in the words of FDA: "Jalapenos may be contaminated with Salmonella."Whole Foods Mild Guacamole Dip recall: WFM Purchasing, LP, Class I (FDA event 99640)https://recallregister.com/fda/i/99640/recallregister:fda:food/99640Wed, 26 Aug 2026 12:00:00 GMTFDA event 99640, food. Class I. FDA report date: 26 Aug 2026. Recalling firm: WFM Purchasing, LP. Reason for recall, in the words of FDA: "Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella."Get Fresh Produce Jalapeno Peppers recall: GET FRESH PRODUCE, Class I (FDA event 99650)https://recallregister.com/month/2026-08/#fda-99650recallregister:fda:food/99650Wed, 26 Aug 2026 12:00:00 GMTFDA event 99650, food. Class I. FDA report date: 26 Aug 2026. Recalling firm: GET FRESH PRODUCE. Reason for recall, in the words of FDA: "Potential Salmonella contamination"Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride… recall: Spectra Medical Devices, Llc, Class I (FDA event 98777)https://recallregister.com/month/2026-08/#fda-98777recallregister:fda:device/98777Wed, 19 Aug 2026 12:00:00 GMTFDA event 98777, device. Class I. FDA report date: 19 Aug 2026. Recalling firm: Spectra Medical Devices, Llc. Reason for recall, in the words of FDA: "Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance. If the product sterility is compromised, patients may be exposed to microorganisms, endotoxins, or foreign matter. This may trigger inflammatory responses, infections, micro-clots, and organ failure."Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recall: Baxter Healthcare Corporation, Class I (FDA event 99343)https://recallregister.com/fda/i/99343/recallregister:fda:device/99343Wed, 19 Aug 2026 12:00:00 GMTFDA event 99343, device. Class I. FDA report date: 19 Aug 2026. Recalling firm: Baxter Healthcare Corporation. Reason for recall, in the words of FDA: "Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position."Kian Pee Wan Capsules recall: Buy-Herbal, Class I (FDA event 98650)https://recallregister.com/month/2026-08/#fda-98650recallregister:fda:drug/98650Wed, 19 Aug 2026 12:00:00 GMTFDA event 98650, drug. Class I. FDA report date: 19 Aug 2026. Recalling firm: Buy-Herbal. Reason for recall, in the words of FDA: "Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine."Cefazolin in Dextrose recall: Baxter Healthcare Corporation, Class I (FDA event 99463)https://recallregister.com/fda/i/99463/recallregister:fda:drug/99463Wed, 19 Aug 2026 12:00:00 GMTFDA event 99463, drug. Class I. FDA report date: 19 Aug 2026. Recalling firm: Baxter Healthcare Corporation. Reason for recall, in the words of FDA: "Presence of Particulate Matter"Glutathione (MDV) recall: Victory Medical Center Pharmacy, Class I (FDA event 99509)https://recallregister.com/month/2026-08/#fda-99509recallregister:fda:drug/99509Wed, 19 Aug 2026 12:00:00 GMTFDA event 99509, drug. Class I. FDA report date: 19 Aug 2026. Recalling firm: Victory Medical Center Pharmacy. Reason for recall, in the words of FDA: "Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin."Optiray Imaging Bulk Package-350 recall: Liebel-Flarsheim Company LLC, Class I (FDA event 99510)https://recallregister.com/fda/i/99510/recallregister:fda:drug/99510Wed, 19 Aug 2026 12:00:00 GMTFDA event 99510, drug. Class I. FDA report date: 19 Aug 2026. Recalling firm: Liebel-Flarsheim Company LLC. Reason for recall, in the words of FDA: "Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass."Dark Chocolate Coconut Almond Bites recall: Bazzini LLC, Class I (FDA event 99097)https://recallregister.com/fda/i/99097/recallregister:fda:food/99097Wed, 19 Aug 2026 12:00:00 GMTFDA event 99097, food. Class I. FDA report date: 19 Aug 2026. Recalling firm: Bazzini LLC. Reason for recall, in the words of FDA: "Undeclared peanuts"Cross Valley Farms LETTUCE CHOP 4/5# Cross Valley Farms LETTUCE SHRED 1/4"… recall: Taylor Farms de Mexico S. de R.L. de C.V., Class I (FDA event 99453)https://recallregister.com/fda/i/99453/recallregister:fda:food/99453Wed, 19 Aug 2026 12:00:00 GMTFDA event 99453, food. Class I. FDA report date: 19 Aug 2026. Recalling firm: Taylor Farms de Mexico S. de R.L. de C.V. Reason for recall, in the words of FDA: "Potential Cyclospora contamination."Cibus Fresh, Sprig & Sprout recall: Piazza Produce (dba CIBUS Fresh), Class I (FDA event 99470)https://recallregister.com/month/2026-08/#fda-99470recallregister:fda:food/99470Wed, 19 Aug 2026 12:00:00 GMTFDA event 99470, food. Class I. FDA report date: 19 Aug 2026. Recalling firm: Piazza Produce (dba CIBUS Fresh). Reason for recall, in the words of FDA: "Possible Cyclospora Contamination"Grade A Brown In-shell Chicken eggs packaged in the following configurations: 1 recall: MIDWEST POULTRY SERVC C/O H & LELECTRIC, Class I (FDA event 99479)https://recallregister.com/fda/i/99479/recallregister:fda:food/99479Wed, 19 Aug 2026 12:00:00 GMTFDA event 99479, food. Class I. FDA report date: 19 Aug 2026. Recalling firm: MIDWEST POULTRY SERVC C/O H & LELECTRIC. Reason for recall, in the words of FDA: "Possible Salmonella Enteritidis"Aquafaba Powder recall: 529 COMMERCE, LLC, Class I (FDA event 99519)https://recallregister.com/month/2026-08/#fda-99519recallregister:fda:food/99519Wed, 19 Aug 2026 12:00:00 GMTFDA event 99519, food. Class I. FDA report date: 19 Aug 2026. Recalling firm: 529 COMMERCE, LLC. Reason for recall, in the words of FDA: "Undeclared Egg"Ashfiat Alharamain Energy Support 250ml/8fl recall: AKKARCO LLC, Class I (FDA event 98392)https://recallregister.com/month/2026-08/#fda-98392recallregister:fda:food/98392Wed, 12 Aug 2026 12:00:00 GMTFDA event 98392, food. Class I. FDA report date: 12 Aug 2026. Recalling firm: AKKARCO LLC. Reason for recall, in the words of FDA: "Undeclared tadalafil"