Philips recalls Achieva 7.0T MRI systems with model 781240 due to risk of ceiling speakers falling and being pulled by magnetic fields. 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 its Achieva 7.0T MRI systems with model number 781240 because ceiling speakers could fall and be pulled by the magnetic field. This poses a risk of injury if the speaker falls and contacts a person.
The magnetic field in the MRI system can attract metal objects, including ceiling speakers. If a speaker falls, it could be pulled toward the MRI machine and potentially cause injury to anyone nearby.
Medical facilities using Philips Achieva 7.0T MRI systems with model number 781240 are most at risk. Patients and staff near the MRI during operation could be affected if the speaker falls.
Check for the model number 781240 on the Achieva 7.0T MRI system. This recall applies to all systems sold by Philips Medical Systems Nederlands.
Look for the model number 781240 on the Achieva 7.0T MRI system.
The ceiling speakers could fall and be pulled by the magnetic field, posing a risk of injury if they contact a person.
Check the model number on your Achieva 7.0T MRI system. If it matches 781240, contact Philips Medical Systems Nederlands for further instructions.
The recall states there is a potential for injury if the speaker falls and contacts a person, but the remedy is not specified in the record.
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-0897-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0897-2019 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.
