Device recall
Z-2434-2024: Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Wireless…
FDA device recall · Class II · B Braun Medical Inc
Key facts
| Recall number (Z-number) | Z-2434-2024 |
|---|---|
| Recall event | 94890 |
| Product | Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Wireless Model/Catalog Number: 8713031U Software Version: 8713031U Product Description: Perfusor Space Syringe Pump, Infusion Pump, 1 each Component: N/A |
| Product code | FRN |
| Recalling firm | B Braun Medical Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K172831, 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