Philips recalls Achieva 1.5T MRI systems with model 781283 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 1.5T MRI systems with model number 781283 because ceiling speakers could fall and be pulled by the magnetic field. This hazard could cause injury if the speaker falls and strikes someone during use.
The magnetic field in the MRI system can attract metal objects, including ceiling speakers. If a speaker falls, it could strike someone in the room, causing injury.
Healthcare facilities using Philips Achieva 1.5T MRI systems with model 781283 are most at risk. Patients and staff near the MRI room during operation could be affected if the speaker falls.
Check for the model number 781283 on the Achieva 1.5T Conversion MRI system. This recall applies to all systems sold by Philips Medical Systems Nederlands.
Identify the model number on your Achieva 1.5T MRI system to confirm if it is 781283.
Reach out to Philips Medical Systems for guidance on next steps for affected units.
The recall is due to a potential risk where ceiling speakers could fall and be pulled by the MRI's magnetic field, which could cause injury.
The official notice does not specify a fix; affected facilities should contact Philips for guidance.
Check for the model number 781283 on your Achieva 1.5T Conversion MRI system.
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-0907-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0907-2019 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.
