Device recall
Z-2822-2015: ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.
FDA device recall · Class II · MicroAire Surgical Instruments, LLC
Key facts
| Recall number (Z-number) | Z-2822-2015 |
|---|---|
| Recall event | 72106 |
| Product | ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use. |
| Product code | MUU |
| Recalling firm | MicroAire Surgical Instruments, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2016 |
| 510(k) numbers | K113128 |
| FEI number | 2020601 |
At a glance
- 1–9 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