Class II — Invacare Corporation
| Recalling firm | Invacare Corporation dba Invacare America |
|---|---|
| Registered facility | View this company's 7 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Invacare identified that the rail mounting bracket on the G29 full length bed rail was out of specification for entrapment safety. |
| Product | G- Series Beds; G29 full length bed rails assembly |
| Quantity | 2499 units |
| Distribution | US Nationwide Distribution including OH, CO, MO, and NY. |
| Initiated | 2014-12-05 |
| Classified | 2015-02-02 |
| Terminated | 2015-06-18 |
| Recall number | Z-1036-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Invacare Corporation (Z-1036-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/69450/
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