Device recall
Z-0954-2023: CoreLink LLC, FLXFIT 15, 32MM X 8MM, CAGE, REF: AT3208
FDA device recall · Class II · CoreLink LLC
Key facts
| Recall number (Z-number) | Z-0954-2023 |
|---|---|
| Recall event | 91109 |
| Product | CoreLink LLC, FLXFIT 15, 32MM X 8MM, CAGE, REF: AT3208 |
| Product code | MAX |
| Recalling firm | CoreLink LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 20, 2024 |
| 510(k) numbers | K171519 |
| FEI number | 3006494201 |
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