Assist Bed Rail — Class II medical device recall Z-2218-2017
Terminated recall by Invacare Corporation, reported 2017-06-07, distributed in DC. A typographical error was noted within the user manual for the 6632 Assist Bed Rail which could result in the
| Recall number | Z-2218-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Invacare Corporation, Elyria, OH, United States |
| Recall initiated | 2017-04-25 |
| Classified | 2017-06-01 |
| Reported by FDA | 2017-06-07 |
| Terminated | 2018-01-16 |
| Distributed | DC |
| Countries outside the US | AU, CA |
| Quantity | 5,020 units |
Product
Assist Bed Rail - 6632
Reason for recall
A typographical error was noted within the user manual for the 6632 Assist Bed Rail which could result in the Assist Bed Rails being installed incorrectly.
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-2218-2017. 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.