Philips recalls Zenition 50 MRI scanners (model 718096) due to potential fuse blowing during start-up or procedures. Affected units have specific serial numbers listed in the recall notice.
Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.
Philips is recalling certain Zenition 50 MRI scanners (model 718096) because the Mains Control Unit board fuse may blow during system start-up or procedures. This could lead to system failure or safety risks during medical imaging.
The Mains Control Unit board fuse may blow during system start-up or procedures, which could cause the MRI scanner to malfunction. This might lead to system interruptions or safety risks during medical imaging sessions.
Medical facilities that own or use the recalled Philips Zenition 50 MRI scanners (model 718096) are most at risk. Patients using these scanners during procedures may face potential system interruptions.
Check if your Philips Zenition 50 MRI scanner has model number 718096. Affected units have specific serial numbers listed in the recall notice, which include a long list of numbers starting with 792 and ending with 194.
Verify your Philips Zenition 50 MRI scanner model number is 718096.
Reach out to Philips customer support for assistance with the recall process.
Check if your scanner has model number 718096 and one of the specific serial numbers listed in the recall notice.
Contact Philips customer support to determine the next steps for your specific unit.
The recall states potential for the Mains Control Unit board fuse to blow during start-up or procedures, which could cause system interruptions but does not explicitly mention serious injury risks.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0352-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-0352-2025 from Philips. 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.
