Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MED-810A Zemits NDPrime Laser products Recalled by Advance-Esthetic LLC Due to Advance-Esthetic LLC failed to comply with the applicable...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Advance-Esthetic LLC directly.
Affected Products
MED-810A Zemits NDPrime Laser products
Quantity: 19
Why Was This Recalled?
Advance-Esthetic LLC failed to comply with the applicable standards regarding Electronic Product Radiation Control (EPRC) regulations associated with the laser product performance standards and certification. This Recall provides correction by the firm regarding Zemits NdPrime Yag Tattoo Removal Laser. The product requires update or is missing the following in part: remote interlock connector, safety interlocks, manual reset mechanism, beam attenuator, tests for determination of compliance, certification, class IV designation and warning, labels, and labeling.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Advance-Esthetic LLC
Advance-Esthetic LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report