Device recall
Z-2520-2021: 10 ga ARS Decompression Needle, Part Number ZZ-0298
FDA device recall · Class II · North American Rescue LLC.
Key facts
| Recall number (Z-number) | Z-2520-2021 |
|---|---|
| Recall event | 88603 |
| Product | 10 ga ARS Decompression Needle, Part Number ZZ-0298 |
| Product code | GAA |
| Recalling firm | North American Rescue LLC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 19, 2024 |
| FEI number | 3005034064 |
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