Device recall
Z-0906-04: AcuSnare Polypectomy Device, Cook Wilson-Cook Medical GI Endoscopy, 4900…
FDA device recall · Class III · Wilson-Cook Medical Inc
Key facts
| Recall number (Z-number) | Z-0906-04 |
|---|---|
| Recall event | 28903 |
| Product | AcuSnare Polypectomy Device, Cook Wilson-Cook Medical GI Endoscopy, 4900 Bethania Station Road, Winston-Salem, NC 27105. The SASM device prefix denotes Soft AcuSnare Mini. The ASM device prefix denotes Acu Snare Mini. Due to the nitinol core wire, the difference between these two products is… |
| Product code | FDI |
| Recalling firm | Wilson-Cook Medical Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 10, 2004 |
| 510(k) numbers | K851958 |
| FEI number | 1037905 |
At a glance
- 1–9 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