Philips recalls Intera 3.0T Master/Quasar Dual MRI systems (model 781150) due to risk of ceiling speakers falling and being pulled by magnetic fields. No remedy specified in recall notice.
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 3.0T Master/Quasar Dual MRI systems (model 781150) because ceiling speakers could fall and be pulled toward the MRI machine by magnetic fields. This hazard could cause injury if the speakers fall and strike someone.
The MRI system's strong magnetic field can attract metal objects, including ceiling speakers. If these speakers fall, they could strike people or equipment near the MRI machine, potentially causing injury.
Healthcare facilities using Philips Intera 3.0T Master/Quasar Dual MRI systems with model number 781150 are most at risk. Patients and staff near the MRI system could be affected if speakers fall.
Check if your Philips Intera 3.0T Master/Quasar Dual MRI system has model number 781150. This system was sold as a nuclear magnetic resonance imaging device.
Identify if your MRI system has model number 781150 by checking the product label or documentation.
The recall notice does not specify any remedy or fix for this issue.
Check if your Philips Intera 3.0T Master/Quasar Dual MRI system has model number 781150.
The recall notice does not specify any action steps for affected systems.
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-0883-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0883-2019 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.
