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Aerolase Corporation recalls LightPod ERA lasers
Recalled January 15, 2020 · FDA recall Z-0768-2020 · Aerolase
Hazard
This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device · FDA Class II
Units
65
Sold at
US Nationwide Distribution
Description
This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device
Product
LightPod ERA lasers
Manufacturer(s)
Aerolase Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →