Device recall
Z-2436-2024: Brand Name: Perfusor Space Product Name: PERFUSOR SPACE ACM-KIT Model/Catalog…
FDA device recall · Class II · B Braun Medical Inc
Key facts
| Recall number (Z-number) | Z-2436-2024 |
|---|---|
| Recall event | 94890 |
| Product | Brand Name: Perfusor Space Product Name: PERFUSOR SPACE ACM-KIT Model/Catalog Number: 8713040U Product Description: Perfusor Space, Infusion Pump Kit, 1 each Component: N/A |
| Product code | FRN |
| Recalling firm | B Braun Medical Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K092313 |
| 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