Device recall
Z-0253-2018: Nonabsorbable suture anchor system intended to reattach soft tissue to bone in…
FDA device recall · Class II · ConMed Corporation
Key facts
| Recall number (Z-number) | Z-0253-2018 |
|---|---|
| Recall event | 77039 |
| Product | Nonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic surgical procedures may be used in either arthroscopic or open surgical procedures. |
| Product code | MBI |
| Recalling firm | ConMed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 31, 2021 |
| 510(k) numbers | K091549 |
| FEI number | 3001451571 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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