Device recall
Z-2860-2026: Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400…
FDA device recall · Class II · Maquet Critical Care AB
Key facts
| Recall number (Z-number) | Z-2860-2026 |
|---|---|
| Recall event | 99359 |
| Product | Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530 Flow-i C40 6888540 Flow-c 6887700 Flow-e 6887900 |
| Product code | BSZ |
| Recalling firm | Maquet Critical Care AB |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K191027 |
| FEI number | 3002808128 |
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