Device recall
Z-1279-2022: Flow-e Anesthesia System: Intended for use in administering anesthesia while…
FDA device recall · Class I · Getinge Usa Sales Inc
Key facts
| Recall number (Z-number) | Z-1279-2022 |
|---|---|
| Recall event | 90250 |
| Product | Flow-e Anesthesia System : Intended for use in administering anesthesia while controlling the entire ventilation of patient Product Code/REF Number: 6887900 |
| Product code | BSZ |
| Recalling firm | Getinge Usa Sales Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 6, 2024 |
| 510(k) numbers | K191027 |
| FEI number | 3013876692 |
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