FDA Device recall Z-0783-2022
(1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX component to Liko overhea…
- FDA Device
- Class II
- terminated
- Published 2022-03-23
On 2022-03-23 the FDA classified a Class II recall of (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX component to Liko overhea… by Hill Rom, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0783-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-01-14 |
| Published | 2022-03-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Hill Rom |
| Distribution | US |
Product
(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
Reason
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
Identifiers
| code_info | Distributed between 04JAN2021 and 24MAR2021. P/N Product name 3130001 Multirall 200 3301030 LikoGuard L 3301040 L…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, natu |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0783-2022%22
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