Device recall
Z-1850-2019: AUTION HYBRID AU-4050
FDA device recall · Class II · Arkray Factory USA, Inc.
Key facts
| Recall number (Z-number) | Z-1850-2019 |
|---|---|
| Recall event | 82737 |
| Product | AUTION HYBRID AU-4050 |
| Product code | KQO |
| Recalling firm | Arkray Factory USA, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 17, 2020 |
| 510(k) numbers | K121456 |
| FEI number | 1832816 |
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