Liko Standard Slingbar 450 — Class II medical device recall Z-0622-2013
Terminated recall by Hill-Rom, Inc., reported 2013-01-09, distributed nationwide. Liko/Hill-Rom has received reports from facilities which indicate that serious injuries have been received rel
| Recall number | Z-0622-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hill-Rom, Inc., Batesville, IN, United States |
| Recall initiated | 2012-12-06 |
| Classified | 2012-12-31 |
| Reported by FDA | 2013-01-09 |
| Terminated | 2014-11-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 261 units |
Product
Liko Standard Slingbar 450. The Standard Slingbar 450 is a versatile sling bar which can be used for most lifting situations. It can be used with different Liko ceiling and mobile lifts.
Reason for recall
Liko/Hill-Rom has received reports from facilities which indicate that serious injuries have been received related to the Standard Sling bar 450. There have been 6 complaints of injury related to the product over the past 32 years (6 out of 838,687,856 estimated patient uses). One of the injuries was associated with a patient during use, four injuries occurred when the slingbar was not in use wher
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0622-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.