Device recall
Z-1237-2017: Hidrex USA DVP1000
FDA device recall · Class III · Hidrex GmbH
Key facts
| Recall number (Z-number) | Z-1237-2017 |
|---|---|
| Recall event | 76362 |
| Product | Hidrex USA DVP1000 |
| Product code | EGJ |
| Recalling firm | Hidrex GmbH |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 4, 2017 |
| 510(k) numbers | K133033 |
| FEI number | 3008642982 |
At a glance
- 1–9 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