Device recall
Z-0032-2013: Caremor Cliner is labeled in part: "***Manufactured By Winco***Ocala, FL 34474…
FDA device recall · Class II · Winco Mfg., LLC
Key facts
| Recall number (Z-number) | Z-0032-2013 |
|---|---|
| Recall event | 63085 |
| Product | Caremor Cliner is labeled in part: "***Manufactured By Winco***Ocala, FL 34474 www.wincomfg.com***Model No. 535 Serial No. 535A-104522***" Literature: "***Caremor Cliner 5351/5361***Winco***ISO 9001-2008 Certified***Our most comfortable and versatile recliner***Ease of operation, outstanding… |
| 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