Device recall
Z-2068-2026: Mint Lesion; Software Versions: 3.4.0 up to 3.9.5.;
FDA device recall · Class II · Mint Medical GmbH
Key facts
| Recall number (Z-number) | Z-2068-2026 |
|---|---|
| Recall event | 98753 |
| Product | Mint Lesion; Software Versions: 3.4.0 up to 3.9.5.; |
| Product code | LLZ |
| Recalling firm | Mint Medical GmbH |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K142647 |
| FEI number | 3011706018 |
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