Device recall
Z-0660-2020: SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Product…
FDA device recall · Class II · Bellus Medical
Key facts
| Recall number (Z-number) | Z-0660-2020 |
|---|---|
| Recall event | 84154 |
| Product | SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Product Usage: The SKINFUSE Rescue Calming Complex is intend to be used to soothe and calm skin (cosmetic). The SKINFUSE LIFT HG is a hydrogel wound dressing to protect against abrasion and friction during the microneedling… |
| Product code | QAI |
| Recalling firm | Bellus Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 5, 2021 |
| FEI number | 3010392991 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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