FDAAugust 1, 2019device
LightPod Neo Lasers
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device
What to do
FDA enforcement status: Terminated
Brands named
aerolase
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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