Device recall
Z-0270-06: Fusion OMNI- GT * DOME TIP: ERCP Catheter: 6.0 FR./200 CM. 8 Minimum Accessory…
FDA device recall · Class III · Wilson-Cook Medical Inc
Key facts
| Recall number (Z-number) | Z-0270-06 |
|---|---|
| Recall event | 33945 |
| Product | Fusion OMNI- GT * DOME TIP: ERCP Catheter: 6.0 FR./200 CM. 8 Minimum Accessory Channel: 4.2 MM * Disposable Single Use Only * Compatible Wire Guide: .035'' * Rx Only * Wilson-Cook Medical * GI Endoscope * 4900 Betharine Station * Winston-Salem, NC 27105 |
| Product code | FGY |
| Recalling firm | Wilson-Cook Medical Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 7, 2007 |
| FEI number | 1037905 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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