medical Class II Updated 2022-07-20

Spectranetics Corporation recalls Philips Laser System, REF LAS-100, Intermittent Operation, D

Recalled Product

Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC, 50/60HZ, 16 AM

Hazard / Issue

The LAS-100 Laser system may detect an inoperable hardware component during power up, which results in an error code and the system not being operable until code is cleared.

Issued by

FDA

Affected States: AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, NC, NJ, NY, OK, PA, TN, TX, VA
Lot/Code Info: Serial Numbers: 100000 to 100104 UDI/DI: (01)00813132027452
View official government recall

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