Philips recalls Multiva 1.5T MRI systems with model 781074 due to potential ceiling speaker falling and being pulled by magnetic field. 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 781074 because ceiling speakers could fall and be pulled toward the MRI machine by magnetic fields. This poses a risk of injury if the speaker falls and strikes someone.
The magnetic field in MRI systems can attract metal objects. In this case, ceiling speakers might detach and move toward the MRI machine, potentially causing injury if they strike a person.
Healthcare facilities using Philips Multiva 1.5T MRI systems with model 781074 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 781074 on the Multiva 1.5T MRI system. This recall applies to all systems sold by Philips Medical Systems Nederlands.
Look for model number 781074 on the MRI system.
Reach out to Philips Medical Systems for guidance on next steps.
The ceiling speakers could fall and be pulled toward the MRI machine by magnetic fields, posing a risk of injury.
Check the model number and contact Philips Medical Systems for instructions.
The recall states there is a potential for injury if the speaker falls and strikes someone, but no specific injury details are provided.
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-0931-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0931-2019 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.
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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.
