Device recall
Z-1328-2016: MicroAire PAL Cannula Product Usage - Power Aspiration Device
FDA device recall · Class II · MicroAire Surgical Instruments, LLC
Key facts
| Recall number (Z-number) | Z-1328-2016 |
|---|---|
| Recall event | 73373 |
| Product | MicroAire PAL Cannula Product Usage - Power Aspiration Device |
| Product code | GEA |
| Recalling firm | MicroAire Surgical Instruments, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 14, 2017 |
| FEI number | 2020601 |
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