G- Series Beds — Class II medical device recall Z-1036-2015
Terminated recall by Invacare Corporation, reported 2015-02-11, distributed nationwide. Invacare identified that the rail mounting bracket on the G29 full length bed rail was out of specification fo
| Recall number | Z-1036-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Invacare Corporation, Elyria, OH, United States |
| Recall initiated | 2014-12-05 |
| Classified | 2015-02-02 |
| Reported by FDA | 2015-02-11 |
| Terminated | 2015-06-18 |
| Distributed | Nationwide (US) |
| Quantity | 2,499 units |
| Reason classes | specification failure |
| Model numbers | 40121, 40122, 40130, 40131, 40201, 40204, 40205, 40206, 40210, 40211, 40212, 40213, 40214, 40217, 40218, 40219, 40220, 40221, 40224, 40225, 40226, 40227, 40228, 40303, 40304 and 101 more |
Product
G- Series Beds; G29 full length bed rails assembly
Reason for recall
Invacare identified that the rail mounting bracket on the G29 full length bed rail was out of specification for entrapment safety.
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-1036-2015. 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.