Device recall
Z-1541-2014: RetractaBed, Clinical Contour, Med - Mizer Inc..... Model SS 762 ( 76 " bed w/…
FDA device recall · Class II · Med-Mizer, Inc.
Key facts
| Recall number (Z-number) | Z-1541-2014 |
|---|---|
| Recall event | 67871 |
| 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. |
| Product code | FNL |
| Recalling firm | Med-Mizer, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2016 |
| FEI number | 3004976058 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database