Philips recalls CT Vision ACQSIM CT System with serial number 3202 due to potential bracket detachment causing injury to patients or staff during surgery. Affected units may require repair or replacement.
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 CT fluoroscopy system model that could detach from its mounting bracket, potentially injuring patients or medical staff during surgery. This recall is urgent because the detachment risk occurs during normal use without warning.
The monitor bracket assembly shaft may wear without warning, causing it to detach from the suspension arm. If the bracket falls, it could injure anyone in its path during surgery, including patients and medical personnel.
Medical facilities using the Philips CT Vision ACQSIM CT System with serial number 3202 are affected. Patients and medical staff in the operating room are at highest risk during procedures.
Check if your CT Vision ACQSIM CT System has the serial number 3202. This model was sold with the Continuous CT (CCT) option for real-time imaging during surgery.
Immediately cease using the CT Vision ACQSIM CT System with serial number 3202 as it may detach and cause injury.
The recalled system is the Philips CT Vision ACQSIM CT System with serial number 3202.
Check if your CT Vision ACQSIM CT System has the serial number 3202, which was used with the Continuous CT (CCT) option.
Immediately stop using it and contact Philips for instructions on repair or replacement.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0277-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0277-2022 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.
