Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LightPod ERA lasers Recalled by Aerolase Corporation Due to This relates to the standard 21 CFR 1040.10(f)(3)...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aerolase Corporation directly.
Affected Products
LightPod ERA lasers
Quantity: 65
Why Was This Recalled?
This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aerolase Corporation
Aerolase Corporation has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report