Device recall
Z-1986-2025: SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog…
FDA device recall · Class II · Chamberlain Technologies LLC
Key facts
| Recall number (Z-number) | Z-1986-2025 |
|---|---|
| Recall event | 96930 |
| Product | SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog Number: T1415 |
| Product code | FTL |
| Recalling firm | Chamberlain Technologies LLC |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K061445 |
| FEI number | 3015860534 |
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