Reported Jan 15, 2020 · Terminated
LightPod Neo Lasers
Aerolase Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Aerolase Corporation · 777 Old Saw Mill River Rd Ste 205 · Tarrytown, NY · 10591-6703
Is this the product you have?
- LightPod Neo Lasers
- Lot codes and dates
- LightPod Neo Lasers
- Amount recalled
- 649
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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