# FDA recall Z-0783-2022

> **Hill-Rom, Inc.** · Class II · device recall initiated 2022-01-14.

## 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 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

## Distribution

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.

## Key facts

- **Recall number:** Z-0783-2022
- **Recalling firm:** Hill-Rom, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-01-14
- **Report date:** 2022-03-23
- **Termination date:** 2024-11-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Batesville, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0783-2022

## Citation

> AI Analytics. FDA recall Z-0783-2022. Retrieved 2026-09-10 from https://api.ai-analytics.org/recall/Z-0783-2022. Source: US FDA. Licensed CC0.

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