Device recall
Z-0259-2012: Product is a synthetic absorbable suture with needle and labeled as sterile. The…
FDA device recall · Class II · C P Medical Inc.
Key facts
| Recall number (Z-number) | Z-0259-2012 |
|---|---|
| Recall event | 60173 |
| Product | Product is a synthetic absorbable suture with needle and labeled as sterile. The product is sealed inside an inner foil pouch with an outside Tyvek pouch. The outer sterile barrier seal is intact. The product is boxed and shrink wrapped for protection against contamination. The product is a Violet… |
| Product code | NEW |
| Recalling firm | C P Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2011 |
| 510(k) numbers | K013274 |
| FEI number | 3002609049 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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