Device recall
Z-1482-2026: Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog…
FDA device recall · Class II · B Braun Medical Inc
Key facts
| Recall number (Z-number) | Z-1482-2026 |
|---|---|
| Recall event | 98380 |
| Product | Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or… |
| Product code | LCJ |
| Recalling firm | B Braun Medical Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2521402 |
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