Class II — Kreg Medical Inc.
| Recalling firm | KREG MEDICAL, INC. |
|---|---|
| Registered facility | KREG MEDICAL, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during patient use, leaving the patient in a forward tilt position. |
| Product | E-Z WIDER BARIATRIC CHAIR BED; Single Motion Expandable Width Technology |
| Quantity | 59 beds |
| Distribution | Nationwide Distribution including IL and IN. |
| Initiated | 2012-08-02 |
| Classified | 2013-06-05 |
| Terminated | 2018-03-02 |
| Recall number | Z-1480-2013 |
| 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 — Kreg Medical Inc. (Z-1480-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/64927/
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