Spectranetics Corporation: Medical Device Recalls in 2022

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Spectranetics Corporation in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

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Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC, 50/60HZ, 16 AM
Philips Laser System, REF: LAS-100. Used in minimally invasive interventional procedures within the cardiovascular system, and for the removal of problematic pacemaker and defibrillator cardiac leads.