Philips recalls Intera 1.5T Explorer/Nova Dual MRI systems (model 781108) due to potential ceiling speaker falling and being pulled by magnetic field. Affected units may need inspection or repair.
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 certain Intera 1.5T MRI systems because ceiling speakers could fall and be pulled by the magnetic field. This poses a risk of injury if the speaker falls and strikes someone.
The magnetic field in the MRI system can attract metal objects, including ceiling speakers. If a speaker falls, it could strike someone nearby, causing injury.
Medical facilities using Philips Intera 1.5T Explorer/Nova Dual MRI systems with model number 781108 are most at risk. Patients and staff near the MRI room during operation could be affected.
Check for the model number 781108 on the Intera 1.5T Explorer/Nova Dual MRI system. This recall applies to all systems sold by Philips Medical Systems Nederlands.
Look for model number 781108 on the MRI system to confirm if it is affected.
The ceiling speakers could fall and be pulled by the magnetic field, posing a risk of injury if they strike someone.
Check the model number 781108 on the system. If affected, contact Philips Medical Systems for guidance.
The recall states a potential risk of injury from falling speakers, but the exact severity isn't specified.
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-0881-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0881-2019 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.
