Philips recalls Ingenia Ambition X MRI systems (model 781356) due to potential ceiling speaker falling and being pulled by magnetic field. Affected units sold in the US.
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 Ingenia Ambition X MRI systems (model 781356) because ceiling speakers could fall and be pulled by the magnetic field. This poses a risk of injury to people near the machine during operation.
The magnetic field in MRI systems can attract metal objects. Ceiling speakers contain metal parts that could fall and be pulled toward the machine, potentially causing injury to people nearby.
Healthcare facilities using the Ingenia Ambition X MRI systems with model number 781356 are most at risk. Patients and staff near the machine during scans could be affected.
Check for the model number 781356 on the Ingenia Ambition X MRI system. These units were sold in the US and are used in healthcare facilities.
Look for the model number 781356 on the MRI system's label or documentation.
This recall applies to Ingenia Ambition X MRI systems with model number 781356. If your machine has this model, you are affected.
The recall does not specify a remedy, so contact Philips Medical Systems for guidance on next steps.
The hazard description states that ceiling speakers could fall and be pulled by the magnetic field, potentially causing injury to people nearby during MRI scans.
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-0921-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0921-2019 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.
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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.
