Philips recalls Intera 1.5T R11 MRI systems (model 781170) due to risk of ceiling speakers falling and being pulled by magnetic fields. Affected units may need inspection.
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 R11 MRI systems (model 781170) because ceiling speakers could fall and be pulled by the magnetic field. This poses a risk of injury if the speaker falls into the MRI machine.
The magnetic field in the MRI system can attract metal objects, including ceiling speakers. If the speakers fall, they might be pulled into the MRI machine, potentially causing injury to people nearby.
Healthcare facilities using Philips Intera 1.5T R11 MRI systems with model number 781170 are most at risk. Patients and staff near the MRI machine during operation could be affected.
Check for the model number 781170 on the Intera 1.5T R11 MRI system. This recall applies to all systems sold by Philips Medical Systems Nederlands.
Look for the model number 781170 on the Intera 1.5T R11 MRI system.
Yes, the ceiling speakers could fall and be pulled by the magnetic field, potentially causing injury.
Check the model number on your Intera 1.5T R11 MRI system. If it's 781170, contact Philips Medical Systems Nederlands for further instructions.
This recall applies to all Intera 1.5T R11 MRI systems with model number 781170 sold by Philips Medical Systems Nederlands.
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-0886-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0886-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
