Device recall
Z-0478-2016: The Fuhrman Pleural/Pneumopericardial Drainage Set The Fuhrman…
FDA device recall · Class I · Stryker Sustainability Solutions
Key facts
| Recall number (Z-number) | Z-0478-2016 |
|---|---|
| Recall event | 72715 |
| Product | The Fuhrman Pleural/Pneumopericardial Drainage Set The Fuhrman Pleural/Pneumopericardial Drainage Set consists of pigtail catheter, access needle, dilator, and wire guide. The set also includes a multipurpose tubing adapter, and three-way stopcock. |
| Product code | KDQ |
| Recalling firm | Stryker Sustainability Solutions |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 28, 2016 |
| FEI number | 3002615969 |
At a glance
- None 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