Reported Mar 12, 2025 · Ongoing
(1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System; (2) Lumenis Pulse 120H, Moses 2.0 (DOM), REF GA0006802,…
Lumenis, Ltd.
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: LUMENIS, LTD. · Yokneam Ind. Park · Yokne'Am Ilit · N/A
Is this the product you have?
(1) Lumenis Pulse 120H 30 ampREF GA 2009996Laser System(2) Lumenis Pulse 120HMoses 2.0 (DOM)REF GA0006802Laser Systemand (3) Lumenis Pulse 120HREF GA-0008700Laser System
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published GA-200999607290109145518Software version 2.4.1.0. (1) - Serial number 1791, UDI-DI 07290109145518 GA-000680207290109145525(2) - Serial number 1803, UDI-DI 07290109145525 — 07290109145464and (3) REF-GA0008700 - Serial number 1818, UDI-DI 07290109145464. - Amount recalled
- 3 devices
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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