Device recall
Z-2343-2018: 26-Lead Transfer Set for use with APEX Compounding System, Product Catalog…
FDA device recall · Class II · B. Braun Medical, Inc.
Key facts
| Recall number (Z-number) | Z-2343-2018 |
|---|---|
| Recall event | 80231 |
| Product | 26-Lead Transfer Set for use with APEX Compounding System, Product Catalog Number 2112550 |
| Product code | NEP |
| Recalling firm | B. Braun Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2020 |
| 510(k) numbers | K151423 |
| FEI number | 2523676 |
At a glance
- 1–9 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