Philips recalls Intera Achieva 1.5T Nova MRI systems (model 781172) 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 Achieva 1.5T Nova MRI systems (model 781172) because ceiling speakers could fall and be pulled by the magnetic field. This could cause injury if the speaker falls into the MRI machine.
The magnetic field in the MRI system can pull ceiling speakers from their mounts. If a speaker falls, it could become a projectile inside the MRI machine, potentially causing injury to people nearby.
Healthcare facilities using Philips Intera Achieva 1.5T Nova MRI systems with model number 781172 are most at risk. Patients and staff near the MRI machine during operation could be affected.
Check if your Philips Intera Achieva 1.5T Nova MRI system has model number 781172. This recall applies to all systems sold by Philips Medical Systems Nederlands.
Identify the model number on your MRI system's label to confirm if it is 781172.
Reach out to Philips Medical Systems Nederlands for guidance on next steps.
Check if your Philips Intera Achieva 1.5T Nova MRI system has model number 781172 to see if it is affected.
Contact Philips Medical Systems Nederlands for instructions on next steps.
Yes, if a ceiling speaker falls and is pulled by the magnetic field, it could cause injury to people nearby.
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-0888-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0888-2019 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.
