Hill-Rom, Inc. recalls
Every recall we track for Hill-Rom, Inc. — 16 in all, from 2018–2022 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Hill-Rom, Inc. peaked in 2021 (9); 16 since 2017. 6% rated “stop using now”.
All FDA recall records for Hill-Rom, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 1 | 0 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 1 | 3 | 1 | 0 | 5 |
| 2021 | 0 | 8 | 1 | 0 | 9 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Hill-Rom, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Hill-Rom, Inc. recalls
10 shown- Use cautionMedical device
Hill-Rom, Inc. recalls (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX
Hill-Rom recalls specific Traverse Rail Carrier models with potentially loose screws that could cause the rail system to fall, risking injury to caregivers and patients. Affected units include 3101704, 3102514, and other models sold between January 2021 and March 2021.
Hill-RomJan 14, 2022 - Use cautionMedical device
Hill-Rom, Inc. recalls Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
Hill-Rom recalls Liko M230 lifts (model 2050015) sold 2016-2021 with missing bushing causing patient falls. Affected units have serial numbers 5361393-5362761. Contact Hill-Rom for remedy.
Hill-RomDec 23, 2021 - Lower riskMedical device
Hill-Rom Inc. recalls These are communication systems, labeled as: a. NaviCare Nurse Call, Part Numbers: 3.6, 3.7, 3.9 b. Voalte Nurse Call,
Hill-Rom recalls specific nurse call communication systems due to potential failure during reboot cycles. Affected units may become non-functional and require replacement.
Hill-RomOct 14, 2021 - Use cautionMedical device
Hill-Rom, Inc. recalls LikoStretch Mod 600 IC Model Number: 3156065 LikoStretch Mod 600 IC, Wide Model Number: 3156065B (obsolete since
Hill-Rom recalls LikoStretch Mod 600 IC models 3156065 and 3156065B (obsolete since June 2020) due to potential patient sliding during lifts. Affected units may require correction to prevent falls.
Hill-RomAug 11, 2021 - Use cautionMedical device
Hill-Rom, Inc. recalls Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery)
Hill-Rom recalls Affinity Four Birthing Beds (models P3700B-E) with damaged latch mechanism that could cause improper engagement and fall injuries during labor/delivery. Affected units have specific serial numbers listed in the recall notice.
Hill-RomMay 28, 2021 - Stop using nowMedical device
Hill-Rom, Inc. recalls Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare,
Hill-Rom recalls Liko Multirall 200 overhead lifts with serial numbers < 6511935 (made before Sep 24, 2019) due to Q-Link strap lock not engaging properly, risking patient and lift detachment.
Hill-RomDec 18, 2020 - Use cautionMedical device
Hill-Rom, Inc. recalls Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other
Hill-Rom recalls Progressa Bed model P7500 (serials V133AW9885-V142AW0261) manufactured May 2020 due to potential screw failure causing serious injury during medical use.
Hill-RomJun 30, 2020 - Lower riskMedical device
Hill-Rom, Inc. recalls Centrella Smart+ Bed, Catalog Number P7900
Hill-Rom recalls Centrella Smart+ Bed (Catalog P7900) with serial codes from U290PF8145 to V015PF2473 and specific updated codes. The bed's exit system may fail to send remote alerts if previously canceled.
Hill-RomApr 30, 2020 - Use cautionMedical device
Hill-Rom Inc. recalls NaviCare Patient Safety Software Versions 3.5.400-3.9.300. The NaviCare Patient Safety (Patient Safety) Software is
Hill-Rom recalls NaviCare Patient Safety Software versions 3.5.400-3.9.300 due to potential failure to monitor patient bed exits. Affected units include specific bed models with these software versions.
Hill-RomFeb 14, 2020 - Use cautionMedical device
Hill-Rom, Inc. recalls Progressa Bed - AC-powered adjustable hospital bed
Hill-Rom recalls AC-powered adjustable hospital beds from June 2017 due to brake system failure risk. Affected models S159AW9192 to S305AW2321 may cause bed movement and patient injury if brakes malfunction.
Hill-RomJan 12, 2018
Hill-Rom, Inc. recall questions
How many recalls has Hill-Rom, Inc. had?
16 recalls from Hill-Rom, Inc. are on record with U.S. safety agencies, from 2018–2022.
What is the most recent Hill-Rom, Inc. recall?
Hill-Rom, Inc. recalls (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX, dated Jan 14, 2022. Every Hill-Rom, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Hill-Rom, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Hill-Rom, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.