Philips recalls certain CT fluoroscopy ceiling mounts due to potential detachment causing injury. Affected units have specific serial numbers and were sold in the U.S. Learn what to do.
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 specific CT fluoroscopy ceiling mounts that could detach and cause injury to people nearby. This recall affects medical equipment used in surgeries and imaging procedures.
The monitor bracket assembly may wear without being noticed, causing it to detach from the suspension arm. If it falls, it could injure anyone in its path, including patients, staff, or bystanders during surgery.
Healthcare professionals and patients using the recalled equipment are at risk. Medical facilities that use this specific model are most vulnerable.
Check for the serial number 7084 7145 758: This is the only identifier provided for affected units. The product is part of the Gemini TF 16 system and was sold in the U.S.
Inspect the monitor bracket assembly for signs of wear or looseness that could cause detachment.
Reach out to Philips for guidance on whether your unit is affected and what to do next.
Yes, the monitor bracket could detach and cause injury to people nearby during use.
Check for the serial number 7084 7145 758 and contact Philips for further instructions.
The affected units have the specific serial number 7084 7145 758 and are part of the Gemini TF 16 system.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0280-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0280-2022 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.
