Device recall
Z-2267-2019: Smith & Nephew Negative Pressure Wound Therapy 15FR Channel Wound Drain PN…
FDA device recall · Class II · Degania Silicone, Ltd.
Key facts
| Recall number (Z-number) | Z-2267-2019 |
|---|---|
| Recall event | 83287 |
| Product | Smith & Nephew Negative Pressure Wound Therapy 15FR Channel Wound Drain PN: 02872 An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than blood vessels, drain fluids from body cavities… |
| Product code | GBX |
| Recalling firm | Degania Silicone, Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 22, 2020 |
| FEI number | 7682 |
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