Philips recalls certain Gemini TF 64 CT ceiling mounts due to potential bracket detachment during use, risking injury to patients or staff. Affected units have 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 ceiling mounts that could detach and cause injury if they fall. This is a safety issue for medical staff and patients during 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, operators, or bystanders.
Healthcare facilities using the recalled Gemini TF 64 CT ceiling mounts are most at risk. Patients and medical staff during procedures could be injured if the mount detaches.
Check for the Gemini TF 64 system with serial numbers 7141, 7218, 7229, or 7245. These mounts were sold with Philips CT products.
Look for the serial numbers 7141, 7218, 7229, or 7245 on the product label.
The monitor bracket assembly may wear without being noticed, potentially causing it to detach and injure people in its path.
Check the serial number on the product. If it matches 7141, 7218, 7229, or 7245, contact Philips for further instructions.
Yes, if the bracket detaches and falls, it could cause injury to patients, operators, bystanders, or service personnel.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0281-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0281-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
