Device recall
Z-1130-2026: Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR…
FDA device recall · Class II · LEASEIR TECHNOLOGIES SLU
Key facts
| Recall number (Z-number) | Z-1130-2026 |
|---|---|
| Recall event | 98176 |
| Product | Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b Software Version: 1.5.0.0 Product Description: The Leaseir MHR Xcell is a surgical laser instrument for use in general and plastic surgery and dermatology, intended for hair removal and treatment of pseudo… |
| Product code | GEX |
| Recalling firm | LEASEIR TECHNOLOGIES SLU |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K214049 |
| FEI number | 3023344928 |
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