Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Laser System Recalled by Spectranetics Corporation Due to The LAS-100 Laser system may detect an inoperable...
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 Spectranetics Corporation directly.
Affected Products
Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC, 50/60HZ, 16 AM
Quantity: 105 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 27 states: AZ, AR, CA, CO, CT, FL, GA, HI, IL, IN, IA, KS, LA, ME, MD, MA, MI, MN, MO, NJ, NY, NC, OK, PA, TN, TX, VA
About Spectranetics Corporation
Spectranetics Corporation has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report