Device recall
Z-0780-03: Vision Hollow Fiber Oxygenator
FDA device recall · Class II · Gish Biomedical Inc
Key facts
| Recall number (Z-number) | Z-0780-03 |
|---|---|
| Recall event | 26039 |
| Product | Vision Hollow Fiber Oxygenator |
| Recalling firm | Gish Biomedical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 9, 2004 |
| 510(k) numbers | K961530 |
| FEI number | 2021836 |
At a glance
- 1–9 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