Device recall
Z-3018-2020: 4 In. Flat Responder Emergency Trauma Dressing part number 30-0171, packaged in…
FDA device recall · Class II · North American Rescue LLC.
Key facts
| Recall number (Z-number) | Z-3018-2020 |
|---|---|
| Recall event | 86340 |
| Product | 4 In. Flat Responder Emergency Trauma Dressing part number 30-0171, packaged in kits labeled as follows: a) M-FAK Mini First Aid Kit; Kit Product Code: 80-0890 b) M-FAK Mini First Aid Kit, with Bleeding Control Dressing; Kit Product Code: 80-0891 c) M-FAK Mini First Aid Kit, Advance; Kit Product… |
| Product code | FQM |
| Recalling firm | North American Rescue LLC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 31, 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