Device recall
Z-0009-2023: Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive…
FDA device recall · Class II · B Braun Medical Inc
Key facts
| Recall number (Z-number) | Z-0009-2023 |
|---|---|
| Recall event | 90830 |
| Product | Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arterial access. |
| Product code | FOZ |
| Recalling firm | B Braun Medical Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K020785 |
| FEI number | 3003218564 |
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