Philips recalls Intera 1.5T CV MRI systems (model 781107) 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 Intera 1.5T CV MRI systems (model 781107) because ceiling speakers could fall and be pulled toward the MRI machine by magnetic fields. This poses a risk of injury if the speakers hit someone or equipment.
The MRI machine's strong magnetic field can attract metal objects, including ceiling speakers. If these speakers fall, they might hit people or equipment, causing injury or damage.
Healthcare facilities using Philips Intera 1.5T CV MRI systems with model number 781107 are most at risk. Patients and staff near the MRI machine during operation could be affected if the speakers fall.
Check for the model number 781107 on the Intera 1.5T CV MRI system. This recall applies to all units sold by Philips Medical Systems Nederlands.
Look for the model number 781107 on the Intera 1.5T CV MRI system.
The ceiling speakers could fall and be pulled toward the MRI machine by magnetic fields, posing a risk of injury.
Check the model number on your system. If it's 781107, contact Philips Medical Systems Nederlands for instructions.
The recall states there is a potential for injury if the speakers fall and hit someone or equipment, but no specific injury cases are reported.
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-0880-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0880-2019 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.
