Philips Medical Systems recalls its MR-OR 3.0T MRI systems (model 781438) due to potential ceiling speaker falling and being pulled by magnetic fields. Affected units may need inspection or repair.
There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
Philips Medical Systems is recalling its MR-OR 3.0T MRI systems (model 781438) because ceiling speakers could fall and be pulled by the magnetic field. This poses a risk of injury if the speaker falls and strikes someone.
The magnetic field in the MRI system can attract metal objects, including ceiling speakers. If a speaker falls, it could strike someone nearby, causing injury.
Healthcare facilities using Philips MR-OR 3.0T MRI systems with model number 781438 are most at risk. Patients and staff near the MRI room during operation could be affected.
Check for the model number 781438 on the MRI system. This recall applies to all units sold by Philips Medical Systems Nederlands.
Look for the model number 781438 on the MRI system to confirm if it is affected.
Yes, the ceiling speakers could fall and be pulled by the magnetic field, potentially causing injury if they strike someone.
Check the model number 781438 on the MRI system. If affected, contact Philips Medical Systems for further instructions.
This recall applies to all MR-OR 3.0T MRI systems with model number 781438 sold by Philips Medical Systems Nederlands.
We’ve drafted a message you can send Philips Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0925-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0925-2019 from Philips Medical Systems. 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.