Device recall
Z-0778-2013: PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011…
FDA device recall · Class II · Winco Mfg., LLC
Key facts
| Recall number (Z-number) | Z-0778-2013 |
|---|---|
| Recall event | 63651 |
| Product | PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012. A multi position recliner with a steel frame used primarily in clinics, hospitals, and treatment centers for recovery, dialysis, oncology, examination, infusion. |
| Product code | INM |
| Recalling firm | Winco Mfg., LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2013 |
| FEI number | 1027229 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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