LUMENIS, LTD.: Medical Device Recalls in 2025

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by LUMENIS, LTD. in 2025. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

OtoLase Starter Kit; UPN: AC-2003748. Indicated for a variety of surgical uses including ablation, coagulation, incision, excision, and vaporization of soft tissue.
(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.