KayserBetten model IDA beds Product Usage: BED — Class II medical device recall Z-0522-2014
Terminated recall by mobility unlimited inc, reported 2013-12-25, distributed nationwide. Some joints on the doors of a limited number of IDA beds may loosen or separate over time which can cause the
| Recall number | Z-0522-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | mobility unlimited inc, Allentown, PA, United States |
| Recall initiated | 2013-04-11 |
| Classified | 2013-12-16 |
| Reported by FDA | 2013-12-25 |
| Terminated | 2014-10-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 33 beds |
Product
KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL
Reason for recall
Some joints on the doors of a limited number of IDA beds may loosen or separate over time which can cause the doors to drop outward and cause injury.
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-0522-2014. 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.