Philips recalls MR 7700 MRI systems with product numbers 782120 and 782130 due to potential smoke detector bypass during power cycling, which could lead to fire hazards.
The system operator is able to bypass the SmokeDetector Interlock system locking mechanism after a smoke detection by power cycling the system.
Philips is recalling specific models of their MR 7700 MRI systems because users can bypass the smoke detector safety feature by restarting the system. This could allow smoke to enter the machine and cause a fire.
The system's smoke detector safety feature can be disabled by restarting the machine. This allows smoke to enter the MRI room, which could lead to a fire if the system is not properly monitored.
Users of Philips MR 7700 MRI systems with product numbers 782120 or 782130 are affected. Medical facilities using these systems are most at risk due to the potential fire hazard.
Check for product numbers 782120 or 782130 on the MRI system. Serial numbers for these models include specific sequences listed in the recall notice.
Verify if the system can be restarted to bypass the smoke detector safety feature.
Philips recalls these MRI systems because users can bypass the smoke detector safety feature by restarting the system, which could lead to fire hazards.
Product numbers 782120 and 782130 are affected.
Check for product numbers 782120 or 782130 on the MRI system. Serial numbers for these models include specific sequences listed in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2397-2023 — Philips Philips Hello, I own a Philips that is covered by recall Z-2397-2023 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.