Device recall
Z-0802-2022: 20522 Vitale Silver calcium Alginate Dressings 2x2, 10/box
FDA device recall · Class III · CellEra LLC
Key facts
| Recall number (Z-number) | Z-0802-2022 |
|---|---|
| Recall event | 89453 |
| Product | 20522 Vitale Silver calcium Alginate Dressings 2x2, 10/box |
| Product code | FRO |
| Recalling firm | CellEra LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 16, 2023 |
| FEI number | 3007594734 |
At a glance
- None 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