Class II — Med-Mizer, Inc.
| Recalling firm | MED-MIZER, INC |
|---|---|
| Registered facility | MED-MIZER, INC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | All configurations of the SS Retractabed, Clinical Contour, made prior to June 7, 2008 may have had insufficient welding on the foot cross tube. This tube is responsible for holding the two support rails together when using the foot side rails and keeps them from separating from the frame. If the weld on the tube breaks, it can lead to bed collapse or the rollers coming out of the channel on t |
| Product | RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 801, 802, 803, 803A: 80 " bed with 1, 2, or 3, motors and autocontour 120 V, ...Max Safe Working Load 450 LBS. Acute/Longterm Care AC Powered Adjustable Bed for geriatric care. |
| Quantity | 2980 |
| Distribution | USA (nationwide) |
| Initiated | 2014-04-18 |
| Classified | 2014-05-02 |
| Terminated | 2016-05-23 |
| Recall number | Z-1543-2014 |
| 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 — Med-Mizer, Inc. (Z-1543-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/67871/
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