Philips recalls CT scanners with software version 4.8.0.10430 due to unintended motion that may cause collisions with patients or operators. Affected models include specific serial numbers and UDI codes. No remedy is listed in the recall notice.
Unintended motion issues related to Interventional Control that may lead to collision of the Gantry/table with the operator or patient.
Philips is recalling certain models of their Brilliance CT Big Bore computed tomography scanners with software version 4.8.0.10430. The issue involves unintended motion in the Interventional Control system that could lead to collisions with patients or operators. This recall does not include a remedy in the official notice.
The software version 4.8.0.10430 has unintended motion in the Interventional Control system, which may cause the gantry or table to collide with patients or operators during procedures. This could result in injury if the motion occurs during use.
Healthcare facilities that own or use the affected CT scanners are most at risk. Patients and operators during scans could be impacted if the motion issue occurs.
Check for the model numbers 728242, 728243, or 728244 and the specific serial numbers listed in the UDI codes. The affected software version is 4.8.0.10430.
Verify if your CT scanner has software version 4.8.0.10430 by checking the device settings or documentation.
The recall notice does not list any remedy or fix for this issue.
The affected models include specific serial numbers and UDI codes listed in the recall notice, such as model numbers 728242, 728243, and 728244 with software version 4.8.0.10430.
Check the software version in your CT scanner's settings or documentation. If it matches 4.8.0.10430, it is affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1660-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1660-2025 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.
