Device recall
Z-0823-2018: REVOLVE ADVANCED ADIPOSE SYSTEM, for aspiration, harvesting, filtering, and…
FDA device recall · Class II · LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC
Key facts
| Recall number (Z-number) | Z-0823-2018 |
|---|---|
| Recall event | 79136 |
| Product | REVOLVE ADVANCED ADIPOSE SYSTEM, for aspiration, harvesting, filtering, and transferring of autologous adipose tissue for aesthetic body contouring. |
| Product code | MUU |
| Recalling firm | LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 7, 2018 |
| 510(k) numbers | K120902 |
| FEI number | 1000306051 |
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