Philips LAS-100 Laser systems with serial numbers 100000-100104 may intermittently stop working due to hardware errors during power-up. Affected units require specific troubleshooting to resolve intermittent operation issues.
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.
Philips LAS-100 Laser systems with serial numbers 100000 to 100104 may stop working intermittently after power-up due to hardware errors. This could prevent the system from operating until an error code is cleared, potentially disrupting medical procedures.
The system may detect a failing hardware component during startup, causing it to display an error code and become inoperable until the code is cleared. This intermittent malfunction could disrupt medical procedures but does not cause physical injury.
Medical facilities using Philips LAS-100 Laser systems with serial numbers 100000 to 100104 are most likely affected. Patients undergoing procedures with these systems may experience temporary interruptions in treatment.
Check for serial numbers between 100000 and 100104 on the Philips LAS-100 Laser system. The system operates on 100-240 VAC power with 50/60Hz frequency.
Look for error codes displayed during power-up that prevent the system from operating until cleared.
The recalled product is the Philips LAS-100 Laser system with serial numbers 100000 to 100104.
Check if your system has a serial number between 100000 and 100104. The system operates on 100-240 VAC power with 50/60Hz frequency.
No, the system may continue to operate after clearing the error code, but it may stop working intermittently during power-up.
We’ve drafted a message you can send Spectranetics to request your refund or repair — edit it as you like.
Subject: Recall Z-1351-2022 — Spectranetics Spectranetics Hello, I own a Spectranetics that is covered by recall Z-1351-2022 from Spectranetics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
