Device recall
Z-2294-2016: Endotine Transbleph 3.5 (CFD-080-0167)
FDA device recall · Class II · MicroAire Surgical Instruments, LLC
Key facts
| Recall number (Z-number) | Z-2294-2016 |
|---|---|
| Recall event | 74222 |
| Product | Endotine Transbleph 3.5 (CFD-080-0167) |
| Product code | HWC |
| Recalling firm | MicroAire Surgical Instruments, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 12, 2016 |
| 510(k) numbers | K042796 |
| FEI number | 2020601 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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