Philips recalls Enterprise 1.5T MRI systems (model 781145) due to risk of ceiling speakers 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 is recalling its Enterprise 1.5T MRI systems (model 781145) because ceiling speakers could fall and be pulled toward the MRI machine by magnetic fields. This poses a risk of injury if the speakers fall and hit someone.
The MRI machine's strong magnetic field can attract metal objects, including ceiling speakers. If the speakers detach and fall, they could strike someone in the room, causing injury.
Healthcare facilities using Philips Enterprise 1.5T MRI systems (model 781145) are affected. Staff and patients near the MRI room during operation are at risk if speakers fall.
Check for the model number 781145 on the Enterprise 1.5T MRI system. This recall applies to all units sold by Philips Medical Systems Nederlands.
Look for the model number 781145 on the Enterprise 1.5T MRI system.
The recall is due to a potential risk where ceiling speakers could fall and be pulled toward the MRI machine by magnetic fields.
Check the model number on your Enterprise 1.5T MRI system. If it's 781145, contact Philips Medical Systems Nederlands for instructions.
The recall states there is a potential for ceiling speakers to fall and be pulled by magnetic fields, which could cause injury if they strike someone.
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-0882-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0882-2019 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.
