Class II — Potential Health Hazard

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...

Date: November 6, 2013
Company: Candela Corporation
Status: Terminated
Source: FDA (Device)

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.

Affected (51 states)Not affected

About Candela Corporation

Candela Corporation has 5 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report