Philips recalls Mammotrak 1.5T diagnostic coils due to potential patient harm during MRI scans. Affected units have specific serial numbers; contact Philips for details.
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Philips is recalling Mammotrak 1.5T diagnostic coils that could harm patients during MRI scans. This recall affects specific serial numbers and requires immediate attention to prevent injury.
The coil may cause patient harm during MRI scan preparation or execution due to a potential safety issue. This could lead to injury if the coil malfunctions during the procedure.
Patients undergoing MRI scans with the recalled Mammotrak 1.5T coils are at risk. Healthcare providers using these coils for diagnostic purposes should also stop use immediately.
Check the serial number on the coil, which starts with 79, 124, 71, 179, 124, 182, 45, 43, 178, 171, 181, 53, 40, 52, 69, 187, 95. The product was sold under Philips North America.
Immediately stop using the Mammotrak 1.5T coil if it has the specified serial numbers.
The coil may cause patient harm during MRI scan preparation or execution due to a potential safety issue.
Check the serial number on the coil, which starts with 79, 124, 71, 179, 124, 182, 45, 43, 178, 171, 181, 53, 40, 52, 69, 187, 95.
Immediately stop using the coil and contact Philips for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0541-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-0541-2025 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.
