Philips recalls certain CT fluoroscopy ceiling mounts due to potential monitor detachment during use, risking injury to patients or staff. Affected units include Gemini GXL 16-slice systems with specific serial numbers.
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 patients, operators, or bystanders. This recall affects medical imaging equipment used in hospitals and clinics.
The monitor bracket assembly may wear without being noticed, causing it to detach from the suspension arm. If the bracket falls, it could injure anyone in its path during medical procedures.
Healthcare facilities using the affected Philips CT fluoroscopy ceiling mounts are most at risk. Patients and medical staff during procedures could be injured if the monitor detaches.
Check for the specific Gemini GXL 16-slice system with serial number 4165. This recall applies to Philips CT fluoroscopy ceiling mounts sold with the CCT Arm DVI Option.
Inspect the monitor bracket assembly for signs of wear or damage that could cause detachment.
Yes, the monitor bracket assembly could detach and cause injury to patients, operators, or bystanders if it falls during use.
Check for the specific Gemini GXL 16-slice system with serial number 4165. This recall applies to Philips CT fluoroscopy ceiling mounts with the CCT Arm DVI Option.
Inspect the monitor bracket assembly for signs of wear or damage. If you find issues, contact Philips for further guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0278-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0278-2022 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.
