Device recall
Z-0808-2025: Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500…
FDA device recall · Class II · Aerin Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0808-2025 |
|---|---|
| Recall event | 95832 |
| Product | Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack), sterile. |
| Product code | GEI |
| Recalling firm | Aerin Medical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K200300 |
| FEI number | 3011625895 |
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