Philips recalls SmartPath to dStream 1.5T MRI systems (model 781260) 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 SmartPath to dStream 1.5T MRI systems (model 781260) because ceiling speakers could fall and be pulled by the magnetic field. This could cause injury if the speaker moves into a patient or operator.
The MRI's strong magnetic field can attract metal objects, including ceiling speakers. If the speaker falls, it might hit a patient or staff member, causing injury.
Healthcare facilities using Philips SmartPath to dStream 1.5T MRI systems with model number 781260 are most at risk. Patients and staff near the MRI room could be affected if the speaker falls.
Check for the model number 781260 on the SmartPath to dStream 1.5T MRI system. This recall applies to all units sold by Philips Medical Systems Nederlands.
Look for model number 781260 on the SmartPath to dStream 1.5T MRI system.
The ceiling speakers could fall and be pulled by the MRI's magnetic field, potentially causing injury to patients or staff.
Check the model number on your system. If it's 781260, contact Philips Medical Systems Nederlands for repair or replacement instructions.
Yes, the potential for ceiling speakers to fall and be pulled by the magnetic field could cause injury if the speaker moves into a patient or staff area.
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-0900-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0900-2019 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.
