Philips recalls Achieva XR 1.5T/3.0T MRI systems (model 781153) due to risk of ceiling speakers falling and being pulled by magnetic fields. Affected units must be checked for this hazard.
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 XR 1.5T and 3.0T MRI systems (model 781153) 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 MRI systems can attract metal objects. In this case, ceiling speakers might detach and be pulled toward the MRI machine, potentially causing injury if they strike a person.
Healthcare facilities using Philips Achieva XR MRI systems with model number 781153 are most at risk. Patients and staff near the MRI room during operation could be affected if the speaker falls.
Check if your Philips Achieva XR MRI system has model number 781153. The recall applies to all systems with this specific model number.
Look for model number 781153 on your Philips Achieva XR MRI system.
The ceiling speakers could fall and be pulled by the magnetic field, potentially causing injury.
Check if your Philips Achieva XR MRI system has model number 781153.
The recall does not specify a remedy, so contact Philips for further instructions.
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-0884-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0884-2019 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.
