FDA recall Z-1130-2026

LEASEIR TECHNOLOGIES SLU · Class II · device

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 folliculitis barbae on all skin types (Fitzpatrick I-VI). The process implies the generation of intense light pulses at specific wavelengths. The specific nature of the energies and pulse durations cause the desired effect (in the hair follicles and oxyhemoglobin in the blood) heating them sufficiently and destroying them without unnecessary damage to surrounding tissue. This is achieved by controlled emission of laser radiation to the target tissue. The system consists of a main console and two interchangeable applicators that delivers pulsed light in the range of 800-820nm with a peak in the 810nm in different spot sizes. Two of the applicators emitting radiation at 810 nm wavelength for two a

Reason for recall

The console label for affected devices is missing the "DANGER" symbol.

Distribution

US Nationwide distribution in the states of Austin, Texas.

Key facts

Status
Completed
Initiation date
2025-12-15
Report date
2026-01-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Gijon, Spain

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1130-2026