RetractaBed — Class II medical device recall Z-1541-2014
Terminated recall by Med-Mizer, Inc., reported 2014-05-14, distributed nationwide. All configurations of the SS Retractabed, Clinical Contour, made prior to June 7 2008 may have had insufficien
| Recall number | Z-1541-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Med-Mizer, Inc., Batesville, IN, United States |
| Recall initiated | 2014-04-18 |
| Classified | 2014-05-02 |
| Reported by FDA | 2014-05-14 |
| Terminated | 2016-05-23 |
| Distributed | Nationwide (US) |
| Quantity | 191 |
| Model numbers | 200000, 300000-300191, 400000-40103, 762, 763, 763A |
Product
RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 762 ( 76 " bed w/ 2 motors); 763 (3 motors); 763 A ( 3 motors, autocontour) 120 V, ...Max Safe Working Load 450 LBS. Acute/Longterm Care AC Powered Adjustable Bed for geriatric care.
Reason for recall
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 th
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.