Device recall
Z-3263-2024: eakin Cohesive seal, small, Model Number 839002, ostomy barrier seal
FDA device recall · Class III · T.G. Eakin Limited
Key facts
| Recall number (Z-number) | Z-3263-2024 |
|---|---|
| Recall event | 95241 |
| Product | eakin Cohesive seal, small, Model Number 839002, ostomy barrier seal |
| Product code | EXE |
| Recalling firm | T.G. Eakin Limited |
| Recall class | Class III |
| Status | Open, Classified |
| FEI number | 1000339531 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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