Aerolase Corporation Recalls

FDA
1
Total Recalls
1
Agencies
Mar 2021
First Recall
Mar 2021
Latest Recall

Showing 1-1 of 1 recalls

FDA

LightPod ERA lasers

This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device

Aerolase notified all customers to whom such product was delivered. Customer will be informed that the firm plan to provide immediately, and without charge, a remote interlock connector for use with their Aerolase lasers. For questions contact Aerolase in Tarrytown, NY at information@aerolase.com or 914-345-8300.