Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Candela Laser GentleLase Pro Recalled by Candela Corporation Due to Unintended single pulse maybe emitted to handpiece prior...
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 Candela Corporation directly.
Affected Products
Candela Laser GentleLase Pro, Powered Laser Surgical Instrument for dermatological use - Model number: 9914-00-9015. and Candela Laser GentleLase Pro LE, Model number: 9914-00-9040
Quantity: 1258 units
Why Was This Recalled?
Unintended single pulse maybe emitted to handpiece prior to pressing of trigger or footswitch and cause injury.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Candela Corporation
Candela Corporation has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report