Device recall
Z-0312-03: Spiral Gold Hollow Fiber Oxygenator with Duraflow Treatment, a hollow fiber…
FDA device recall · Class II · Jostra-Bentley Corporation
Key facts
| Recall number (Z-number) | Z-0312-03 |
|---|---|
| Recall event | 25002 |
| Product | Spiral Gold Hollow Fiber Oxygenator with Duraflow Treatment, a hollow fiber membrane oxygenator. |
| Recalling firm | Jostra-Bentley Corporation |
| Recall class | Class II |
| Status | Completed |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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