medical Class II Updated 2020-01-15

Aerolase Corporation recalls LightPod ERA lasers

Recalled Product

LightPod ERA lasers

Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: LightPod ERA Lasers
View official government recall

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