Philips recalls Multiva 1.5T MRI systems with model 781073 due to risk of ceiling speakers falling and being pulled by magnetic fields. Affected units may need repair or replacement.
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 is recalling its Multiva 1.5T MRI systems with model number 781073 because ceiling speakers could fall and be pulled by the magnetic field. This hazard could cause injury if the speaker falls into the MRI machine.
The magnetic field in the MRI system can pull ceiling speakers from their mounting. If a speaker falls, it could enter the MRI machine and cause injury to people nearby.
Healthcare facilities using Philips Multiva 1.5T MRI systems with model 781073 are most at risk. Patients and staff near the MRI machine during operation could be affected if the speaker falls.
Check for the model number 781073 on the Multiva 1.5T 16 R5 (ZBO) MRI system. This recall applies to all units sold by Philips Medical Systems Nederlands.
Look for the model number 781073 on the Multiva 1.5T 16 R5 (ZBO) MRI system.
Contact Philips Medical Systems Nederlands for repair or replacement options.
The ceiling speakers could fall and be pulled by the magnetic field, potentially causing injury.
Check for the model number 781073 on the Multiva 1.5T 16 R5 (ZBO) MRI system.
Contact Philips Medical Systems Nederlands for repair or replacement options.
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-0872-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0872-2019 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.
