Philips recalls Achieva 3.0T TX-series MRI systems (model 781278) 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 3.0T TX-series MRI systems (model 781278) because ceiling speakers could fall and be pulled toward the MRI machine by magnetic fields. This poses a risk of injury if the speakers hit people or equipment.
The magnetic field in MRI systems can attract metal objects, including ceiling speakers. If these speakers fall, they might be pulled toward the MRI machine, potentially causing injury to people or damage to equipment.
Healthcare facilities using Philips Achieva 3.0T TX-series MRI systems with model number 781278 are most at risk. Patients and staff near the MRI machine during operation could be affected.
Check if your Philips Achieva 3.0T TX-series MRI system has model number 781278. This recall applies to all systems sold by Philips Medical Systems Nederlands.
Identify the model number on your MRI system to confirm if it is 781278.
Reach out to Philips Medical Systems Nederlands for guidance on next steps.
No, this recall specifically applies to Achieva 3.0T TX-series systems with model number 781278.
Check the model number on your MRI system; affected units have model number 781278.
Contact Philips Medical Systems Nederlands for instructions on next steps.
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-0906-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0906-2019 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.
