Device recall
Z-1520-2011: VCare Vaginal-Cervical Ahluwalia's Retractor-Elevator devices. The VCare IFU is…
FDA device recall · Class III · ConMed Corporation
Key facts
| Recall number (Z-number) | Z-1520-2011 |
|---|---|
| Recall event | 57841 |
| Product | VCare Vaginal-Cervical Ahluwalia's Retractor-Elevator devices. The VCare IFU is packaged one per carton of eight VCare Pouched Devices. The Instructions for Use is an 8.5" x 12" 12-page booklet and is packed loose in the carton. Only the carton will have to be opened to replace the old IFU; there is… |
| Product code | L |
| Recalling firm | ConMed Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 30, 2012 |
| 510(k) numbers | K071907 |
| FEI number | 3001451571 |
At a glance
- 1–9 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