Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
(1) Lumenis Pulse 120H 30 amp Recalled by LUMENIS, LTD. Due to The initial current in certain chargers may lead...
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 LUMENIS, LTD. directly.
Affected Products
(1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System; (2) Lumenis Pulse 120H, Moses 2.0 (DOM), REF GA0006802, Laser System; and (3) Lumenis Pulse 120H, REF GA-0008700, Laser System.
Quantity: 3 devices
Why Was This Recalled?
The initial current in certain chargers may lead to overheating and damage to the power resistors on the Alternating Current (AC) controller during the power-on sequence of the laser system, resulting in the laser system to not power on.
Where Was This Sold?
This product was distributed to 1 state: PA
About LUMENIS, LTD.
LUMENIS, LTD. 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