Device recall
Z-3177-2011: Monomid Non-Absorbable Suture are blue, monofilament synthetic absorbable…
FDA device recall · Class II · C P Medical Inc.
Key facts
| Recall number (Z-number) | Z-3177-2011 |
|---|---|
| Recall event | 59759 |
| Product | Monomid Non-Absorbable Suture are blue, monofilament synthetic absorbable suture, with different sizes and different needle sizes. The products are labeled in parts. These sutures are intended for use in general soft tissue approximation and/or ligation including use in cardiovascular, ophthalmic… |
| Product code | GAR |
| Recalling firm | C P Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 24, 2012 |
| 510(k) numbers | K001173 |
| 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