Device recall
Z-1206-2010: VIPA Veronikis Intra-Fiberoptic Pelvic Assistant, Set Catalog No 350-370. VIPA…
FDA device recall · Class II · Marina Medical Instruments Inc.
Key facts
| Recall number (Z-number) | Z-1206-2010 |
|---|---|
| Recall event | 53501 |
| Product | VIPA Veronikis Intra-Fiberoptic Pelvic Assistant, Set Catalog No 350-370. VIPA Set Includes: VIPA Urethropexy Tip Catalog No. 350-374 (Also sold individually); VIPA Urethropexy Elbow Catalog No. 350-375 (also sold individually); VIPA Vaginal Cuff Tips (small) Catalog No. 350-376 (Also sold… |
| Product code | EXX |
| Recalling firm | Marina Medical Instruments Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 3, 2010 |
| FEI number | 1000124817 |
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