Device recall
Z-1207-2010: VVD Veronikis Vaginal Dilator - Complete Set Catalog No. 270-000. Set Includes…
FDA device recall · Class II · Marina Medical Instruments Inc.
Key facts
| Recall number (Z-number) | Z-1207-2010 |
|---|---|
| Recall event | 53501 |
| Product | VVD Veronikis Vaginal Dilator - Complete Set Catalog No. 270-000. Set Includes: VVD Veronikis Vaginal Dilator - 3cm Tip: Width: 1.00in Catalog No. 270-003 (sold individually) VVD Veronikis Vaginal Dilator - 5cm Tip: Width: 1.00in Cat No. 270-005 (sold individually) VVD Veronikis Vaginal Dilator… |
| 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