Philips recalls TruFlight Select PET/CT System model 882438 due to potential monitor bracket detachment causing injury. Affected units have serial number 17006.
Significant wear of the Monitor Bracket Assembly shaft may go unrecognized could lead to the Monitor Bracket Assembly detaching from the Suspension Arm, and resulting in injury to patient, operator, bystander, or service person located in the path of a falling part
Philips is recalling a specific TruFlight Select PET/CT system model that could detach and cause injury. This risk exists if the monitor bracket becomes loose during use.
The monitor bracket assembly may wear down and become loose without being noticed. If it detaches, it could fall and injure anyone in its path, including patients, operators, or bystanders.
Healthcare professionals using the TruFlight Select PET/CT system with serial number 17006 are most at risk. Patients and others nearby could also be injured if parts detach.
Check for the TruFlight Select PET/CT system with serial number 17006. This model is part of the Philips Continuous CT Fluoroscopy DVI Ceiling Mount.
Inspect the monitor bracket assembly for signs of wear or looseness before use.
This recall applies only to the TruFlight Select PET/CT system with serial number 17006. Check your system's serial number to see if it's affected.
The recall does not specify a remedy. Check for loose bracket assembly and contact Philips for further guidance.
Yes, if the monitor bracket detaches, it could injure patients, operators, or bystanders in the path of a falling part.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0279-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0279-2022 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.
