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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

LEASEIR MHR XCELL Surgical Lasers Recalled for Missing Danger Symbol

Agency Publication Date: January 16, 2026
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Summary

LEASEIR TECHNOLOGIES SLU is recalling 2 units of the LEASEIR MHR XCELL surgical laser instrument (model MHR 110-b). These devices, which are used for hair removal and dermatology treatments, are missing a required "DANGER" symbol on the console label. Consumers should stop using the affected devices and contact the manufacturer or their distributor to arrange for a correction or return.

Risk

The missing symbol fails to provide a necessary safety warning regarding the laser hazard. This lack of proper labeling could lead to accidental exposure to intense light pulses, potentially causing eye or skin injuries.

What You Should Do

  1. This recall involves the LEASEIR MHR XCELL surgical laser (model MHR 110-b, software version 1.5.0.0) with serial numbers C10016 and C10017.
  2. Stop using the recalled device immediately.
  3. Contact the manufacturer, LEASEIR TECHNOLOGIES SLU, or your distributor to arrange for a label correction, replacement, or device return.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls for more information.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: LEASEIR MHR XCELL surgical laser instrument
Variants: Software Version: 1.5.0.0
Model / REF:
MHR 110-b
Serial Numbers:
C10016
C10017
UDI:
08437019546076

Used for hair removal and treatment of pseudo folliculitis barbae on all skin types (Fitzpatrick I-VI).

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98176
Status: Active
Manufacturer: LEASEIR TECHNOLOGIES SLU
Manufactured In: Spain
Units Affected: 2
Distributed To: Texas

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.