CLASS II Device recall · Reported 23 Mar 2022 · FDA Enforcement Report
Traverse Rail Carrier E-System recalled by Hill-Rom
Hill-Rom is recalling Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, Traverse, distributed nationwide in the US. The recall was initiated on 14 Jan 2022 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0783-2022
- FDA event ID
- 89562
- Recalling firm
- Hill-Rom, Batesville, IN
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 14 Jan 2022
- FDA classified
- 11 Mar 2022
- Reported
- 23 Mar 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 14 Jan 2022 | Recall initiated by company | |
| 11 Mar 2022 | Classified by FDA | +56 days |
| 23 Mar 2022 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Traverse rail carriage delivered with non-conforming screws are too short to ensure appropriate installation. There is potential that the screws are unable to secure the traverse rail appropriately and could loosen over time causing the rail system to fall, potentially causing injury to caregivers and/or patients
Product as listed by the FDA
(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 ESYST WIDE 3102517 TR CARR. NORMAL/LOWER. LR 3102506 TR CARRIER WIDE/RAISED ML 3102519 TR CARR. LOW.LR 30MM/PAIR 3102511 TR CARRIER NORMAL, LR 3102531 TRAVERSE RL CARRIER STD/RAISED 3102512 TR CARRIER WIDE, LR 3102532 TRAVERSE RL CARRIER WD/RAISED 3102513 TR CARRIER SLIM, LR 3102562 TR CARRIER, PARALLEL/WIDE
Where it was distributed
Worldwide distribution - US Nationwide and the countries of AT, CA, CZ, DE, DK, ES, FI, FR, GB, HK, IE, IL, IT, JP, NL, NO, NZ, RU, SE, SG, SK.
Questions about this recall
Is Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, Traverse recalled?
Yes. Hill-Rom recalled Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, Traverse on 14 Jan 2022. The recall is Class II and its status is Terminated. Recall number Z-0783-2022.
Why was it recalled?
Traverse rail carriage delivered with non-conforming screws are too short to ensure appropriate installation. There is potential that the screws are unable to secure the traverse rail appropriately and could loosen over time causing the rail system to fall, potentially causing injury to caregivers and/or patients
Which lots are affected?
Distributed between 04JAN2021 and 24MAR2021. P/N Product name 3130001 Multirall 200 3301030 LikoGuard L 3301040 LikoGuard XL 3121001 Likorall 200 3122005 Likorall 242 ES natural 3122005NA Likorall 242 ES natural 3122006 Likorall 242 ES white 3122006NA Likorall 242 ES white 3122009 Likorall 242 S natural 3122009NA Likorall 242 S natural 3122010 Likorall 242 S white 3122010NA Likorall 242 S white 3122007 Likorall 242 ES R2R, natural 3122007NA Likorall 242 ES R2R, natural 3122008 Likorall 242 ES R2R, white 3122008NA Likorall 242 ES R2R, white 3122011 Likorall 242 S R2R, natural 3122011NA Likorall 242 S R2R, natural 3122012 Likorall 242 S R2R, white 3122012NA Likorall 242 S R2R, white 3123001 Likorall 243 ES, natural 3123001NA Likorall 243 ES, natural 3123002 Likorall 243 ES, white 3123002NA Likorall 243 ES, white 3122501 Likorall 250 ES, natural 3122501NA Likorall 250 ES, natural 3122502 Likorall 250 ES, white 3122502NA Likorall 250 ES, white 3124050 Likorall 250 S, IRC, natural
Where was it sold?
Worldwide distribution - US Nationwide and the countries of AT, CA, CZ, DE, DK, ES, FI, FR, GB, HK, IE, IL, IT, JP, NL, NO, NZ, RU, SE, SG, SK.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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