Device recall
Z-1459-2012: ELITE CARE CLINER 6900 (STD)/6910(X-LG) with Swing-Arm products are labeled in…
FDA device recall · Class II · Winco Mfg., LLC
Key facts
| Recall number (Z-number) | Z-1459-2012 |
|---|---|
| Recall event | 61457 |
| Product | ELITE CARE CLINER 6900 (STD)/6910(X-LG) with Swing-Arm products are labeled in part: "***ELITE CARE CLINER 6900/6910***Winco***ISO 9001-2008 Certified***Design, comfort, durability, and value that exceed your expectations.***Attention to detail and concern for comfort and quality, standards that… |
| Product code | INM |
| Recalling firm | Winco Mfg., LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 27, 2012 |
| 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