Philips LAS-100 laser systems used in cardiovascular procedures may enter non-recoverable safe state causing treatment delays. Affected units have specific serial numbers. Contact Philips for details.
Laser System may detect Error 106 or Error 108 System Failures that will cause the system to enter non-recoverable safe state. The user will not be able to proceed until the error is cleared. May result in initiation of treatment delay and/or treatment beyond initial scope and/or unable to treat patient.
Philips LAS-100 laser systems used in cardiovascular procedures may stop working unexpectedly due to Error 106 or 108, potentially delaying or complicating treatments. This recall affects specific units with known serial numbers.
The system may detect Error 106 or 108, causing it to enter a non-recoverable safe state. This prevents the user from proceeding with treatment until the error is cleared, which could delay or extend procedures beyond intended scope.
Healthcare professionals using Philips LAS-100 laser systems for cardiovascular procedures are affected. Those with the specific serial numbers listed in the recall are most at risk.
Check if your Philips LAS-100 system has a serial number starting with 100000 through 100118 or 100120. The software version is 0.5.0.3 and the UDI is 00813132027452.
Verify if your system displays Error 106 or 108 by attempting to run procedures.
Reach out to Philips for guidance on resolving errors and potential recall actions.
The system may detect Error 106 or 108, causing it to enter a non-recoverable safe state that prevents proceeding with treatment until the error is cleared.
Check if your system has a serial number in the list provided and contact Philips for guidance on resolving errors.
Affected units have specific serial numbers starting with 100000 through 100118 or 100120, software version 0.5.0.3, and UDI 00813132027452.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0221-2023 — Philips Philips Hello, I own a Philips that is covered by recall Z-0221-2023 from Philips. 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.
