Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame… — Class II medical device recall Z-1546-2013
Terminated recall by Zimmer, Inc., reported 2013-06-26, distributed nationwide. The bed frame adapter assemblies may have a weak weld where the patient helper adapter mounting bars attach to
| Recall number | Z-1546-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2013-02-14 |
| Classified | 2013-06-14 |
| Reported by FDA | 2013-06-26 |
| Terminated | 2014-05-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 344 units |
| Model numbers | 00-0965-002-01 |
Product
Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame adapter assembly is intended to be used by qualified medical professionals to adapt a patient helper to a hospital bed. The patient helper is used to aid and assist the patient's mobility within a hospital bed and during bed ingress and egress.
Reason for recall
The bed frame adapter assemblies may have a weak weld where the patient helper adapter mounting bars attach to the tube.
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-1546-2013. 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.