Device recall
Z-0774-2024: EVair air compressor, model numbers: M1230849 and M1230847
FDA device recall · Class I · Datex-Ohmeda, Inc.
Key facts
| Recall number (Z-number) | Z-0774-2024 |
|---|---|
| Recall event | 93715 |
| Product | EVair air compressor, model numbers: M1230849 and M1230847 |
| Product code | BTI |
| Recalling firm | Datex-Ohmeda, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 2112667 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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