FDA recall Z-0095-2024

Advance-Esthetic LLC · Class II · device

Product

MED-810A Zemits NDPrime Laser products

Reason for recall

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.

Distribution

US Nationwide Distribution

Key facts

Status
Ongoing
Initiation date
2023-10-09
Report date
2023-10-18
Voluntary/Mandated
FDA Mandated
Location
Fort Lauderdale, FL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0095-2024