Device recall
Z-0819-2022: PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be…
FDA device recall · Class II · B Braun Medical Inc
Key facts
| Recall number (Z-number) | Z-0819-2022 |
|---|---|
| Recall event | 89660 |
| Product | PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be used to configure customized, tailor-made solutions Catalog Number: 8713030U |
| Product code | MEA |
| Recalling firm | B Braun Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 28, 2023 |
| 510(k) numbers | K092313, K172831, K191910 |
| FEI number | 3003218564 |
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