Philips recalls Achieva 3.0T PET MRI systems with model 781477 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 Achieva 3.0T PET MRI systems with model number 781477 because ceiling speakers could fall and be pulled by the magnetic field. This hazard could cause injury if the speaker falls and strikes someone.
The magnetic field in the MRI system can attract metal objects, including ceiling speakers. If the speakers fall, they could strike people in the room, causing injury.
Healthcare facilities using Philips Achieva 3.0T PET MRI systems with model 781477 are most at risk. Patients and staff near the MRI room during operation could be affected.
Check for the model number 781477 on the Achieva 3.0T PET MRI system. This recall applies to all systems sold by Philips Medical Systems Nederlands.
Look for model number 781477 on the Achieva 3.0T PET MRI system.
The ceiling speakers could fall and be pulled by the magnetic field, potentially causing injury.
Check the model number on your system; if it's 781477, contact Philips for further instructions.
Yes, if the speakers fall during use, they could cause injury to people in the MRI room.
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-0927-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0927-2019 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.
