E-Z WIDER BARIATRIC CHAIR BED — Class II medical device recall Z-1480-2013
Terminated recall by Kreg Medical Inc., reported 2013-06-12, distributed nationwide. An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during patient use, leaving the patient in a
| Recall number | Z-1480-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Kreg Medical Inc., Chicago, IL, United States |
| Recall initiated | 2012-08-02 |
| Classified | 2013-06-05 |
| Reported by FDA | 2013-06-12 |
| Terminated | 2018-03-02 |
| Distributed | Nationwide (US) |
| Quantity | 59 beds |
| Serial numbers | KM1000158, KM100109, KM100111, KM100112, KM100113, KM100114, KM100115, KM100116, KM100117, KM100118, KM100119, KM100120, KM100144, KM100145, KM100146, KM100147, KM100148, KM100149, KM100150, KM100151, KM100152, KM100153, KM100154, KM100155, KM100156 and 24 more |
| Model numbers | ASM100100, ASM100104 |
Product
E-Z WIDER BARIATRIC CHAIR BED; Single Motion Expandable Width Technology
Reason for recall
An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during patient use, leaving the patient in a forward tilt position.
Machine access
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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.