Device recall
Z-2972-2024: Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
FDA device recall · Class I · B Braun Medical Inc
Key facts
| Recall number (Z-number) | Z-2972-2024 |
|---|---|
| Recall event | 95093 |
| Product | Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U |
| Product code | FRN |
| Recalling firm | B Braun Medical Inc |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K191910 |
| 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