Food, drugs, devices › Firms
Hill-Rom, Inc. has 28 FDA enforcement events on this register (37 product records) between 2012 and 2022: 28 device; the busiest year was 2016 with 5.
4% of its events are Class I; the most common class is Class II (27). 2 events are listed as ongoing; the recalling firm's address is in IN and NC.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
Initiated Product (first record) Type Class Records Status 14 Jan 2022 (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX component to Liko overhead lift. Intended for to make safe lifting of a patient possible. Affected Devices: 3101704 TRAV RAIL CARR E-SYST STD 3102514 TR CARRIER SLIM/RAISED, LR 3101705 TRAV RAIL CARR… Device Class II 1 Terminated 23 Dec 2021 Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010 Device Class II 2 Ongoing 14 Oct 2021 These are communication systems, labeled as: a. NaviCare Nurse Call, Part Numbers: 3.6, 3.7, 3.9 b. Voalte Nurse Call, Part Number 4.0 *Product was rebranded from NaviCare to Voalte in 2020 Device Class II 1 Terminated 11 Aug 2021 OctoStretch with Stretch Leveller - The combination of this products allows the user to easily adjust/control the center of gravity during lift of patient. Model Number: 3156056 Device Class II 5 Ongoing 28 May 2021 Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market Model Numbers: P3700B, P3700C, P3700D, & P3700E Device Class II 1 Terminated 18 Dec 2020 Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilitation. Affected devices: Liko Multirall 200 (product number 3130001) Universal SlingBar 450 R2R (product number 3156095) Universal SlingBar 350 R2R (product number 3156094)… Device Class I 1 Terminated 30 Jun 2020 Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral Rotation Therapy or Percussion/Vibration… Device Class II 2 Terminated 30 Apr 2020 Centrella Smart+ Bed, Catalog Number P7900 Device Class II 1 Terminated 14 Feb 2020 NaviCare Patient Safety Software Versions 3.5.400-3.9.300. The NaviCare Patient Safety (Patient Safety) Software is compatible with the following beds: 1. VersaCare Revision A-J with upgrade kit Revision K with UCB 1.18 2. Centrella (all versions) 3. Progressa (firmware version 1.15.0.0) Device Class II 1 Terminated 12 Jan 2018 Progressa Bed - AC-powered adjustable hospital bed Device Class II 1 Terminated 23 Feb 2017 TotalCare Bed Systems, Model Numbers P1900, PR1900, and U1900 with 3-Level Patient Position Monitoring and Scale Upgrade Kits, Model Numbers P1947A and P1948A). Device Class II 1 Terminated 9 Aug 2016 Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail systems: Multirall 200, Likorall 200, 242, 243, 250, and LikoGuard L and XL. Device Class II 1 Terminated 15 Jul 2016 Affinity Four Birthing Bed Model P3700 The primary packaging is pictured below, and utilizes a metal packing brace, standard corrugated cardboard and plastic banding. When possible these beds are shipped as a quantity of two (2) together as shown with the nylon strapping. These are shipped in standard freight… Device Class II 1 Terminated 14 Jun 2016 Volker 2080, 2082, S 280 and S 282 series beds with lateral release button. A/C Powered Adjustable Hospital Bed Product Usage: Volker model 2080/3010/3080 nursing beds are intended for the care of residents in rooms in nursing homes, in residential homes for the elderly and in suitable rooms in private residences.… Device Class II 1 Terminated 8 Mar 2016 Liko Universal SlingBars Universal SlingBar" 350, Universal SlingBar" 350 QRH, Universal SlingBar" 350 R2R, Universal SlingBar" 450, Universal SlingBar" 450 QRH, Universal SlingBar" 450 R2R, Universal SlingBar" 600 Universal SlingBar" 600 QRH Component of Liko Lifts Product Usage: Universal SlingBar 350 It is… Device Class II 1 Terminated 20 Jan 2016 Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric Recliner was created to provide an aesthetically pleasing design that will enhance the overall experience for the bariatric patient. Using spring box construction and an exceptionally smooth mechanism, the patient is able to… Device Class II 1 Terminated 7 Oct 2015 Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed Device Class II 1 Terminated 20 Mar 2015 Viking M, L, and XL Mobile Lifts. Non-AC-powered patient lift. Device Class II 1 Terminated 2 Mar 2015 Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece. Device Class II 1 Terminated 26 Jun 2014 Affinity¿ Four Birthing Bed, Product Usage: Product is intended to be used as birthing beds for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market. Device Class II 1 Terminated 30 May 2013 TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum Complete mattress, and AccuMax Quantum Convertible mattress The TotalCare Bed System is intended to provide a patient support ideally suited to be used in health care environments. The TotalCare Bed System may be used in a variety of settings… Device Class II 1 Terminated 30 Apr 2013 SlingBar 350. Designed to meet the needs for lifting humans. Device Class II 4 Terminated 15 Apr 2013 Hill-Rom 1000 Bed, Product No. P1160. The Hill-Rom 1000 Bed is intended for low to moderate acuity patient in the medical surgical area of the hospital. Device Class II 1 Terminated 26 Feb 2013 TotalCare SpO2RT2 bed. Product Usage: Bed, flotation therapy, powered bed may be used in a variety of settings including, but not limited to, acute care, including critical care, step down/progressive care, medical/surgical, high acuity sub-acute care, post anesthesia care unit (PACU), and sections of the emergency… Device Class II 1 Terminated 6 Dec 2012 Liko Standard Slingbar 450. The Standard Slingbar 450 is a versatile sling bar which can be used for most lifting situations. It can be used with different Liko ceiling and mobile lifts. Device Class II 1 Terminated 31 Oct 2012 Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and Masterlift Systems Product Usage - The Overhead Rail System allows overhead lifts to be mounted to the ceiling allowing versatility for use in lifting situations. It can be used with different Liko… Device Class II 1 Terminated 18 Jun 2012 Advanta 2 Bed. The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the hospital. Device Class II 1 Terminated 2 Apr 2012 Affinity Four Birthing Bed P3700 Product Usage: The Affinity, Four Birthing Bed is intended to be used as birthing beds for women of child bearing age in an LDR (Labor, Delivery, Recovery ) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market. They are not intended… Device Class II 1 Terminated
By type and class Class I: 4% of this firm's events; 18% of all events on the register.
Events by year Enforcement events for Hill-Rom, Inc. by year initiated. Questions and answers How many FDA recalls has Hill-Rom, Inc. had? 28 enforcement events (37 product records) on this register, 2012–2022: 28 device.
Are any Hill-Rom, Inc. recalls ongoing? 2 events are listed as ongoing in the current openFDA export.
What class are Hill-Rom, Inc. recalls? 27 Class II, 1 Class I. 4% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from? openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology .