Product Wiki · Recalls · U.S. FDA — Device Enforcement

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 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,

U.S. FDA — Device Enforcement · United States · 2022-01-14 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0783-2022
Date of alert: 2022-01-14
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Hill-Rom, Inc.
Product category: device
Product type: Devices

Reported risk: 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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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