Device recall
Z-1208-2010: VNVD Veronikis Neo Vaginal Dilator - Complete Set Catalog No. 270-100, VNVD…
FDA device recall · Class II · Marina Medical Instruments Inc.
Key facts
| Recall number (Z-number) | Z-1208-2010 |
|---|---|
| Recall event | 53501 |
| Product | VNVD Veronikis Neo Vaginal Dilator - Complete Set Catalog No. 270-100, VNVD Veronikis Neo Vaginal Dilator - 1.5cm Tip:Width:0.625in Catalog No. 270-115 (sold individually), VNVD Veronikis Neo Vaginal Dilator - 2.5cm Tip:Width:0.625in Catalog No. 270-125 (sold individually), VNVD Veronikis Neo… |
| Product code | HDQ |
| 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