Philips recalls Mammotrak Interventional Coil 1.5T devices due to potential patient harm during 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 Interventional Coil 1.5T devices because they could cause patient harm during scans. This affects specific models with certain serial numbers. The recall is for safety reasons to prevent potential injury.
The device may cause harm during scan preparation or execution. The hazard is not clearly explained in the recall notice, so the exact mechanism is unknown.
Medical professionals using the Mammotrak Interventional Coil 1.5T for scans are most at risk. Patients undergoing scans with this device may be harmed.
Check for the serial numbers 69, 82, 143, 64, 77, 87, 76, 81, 134, 124, 141, 103, 135, 138, 73, 72, 131 on the device. The product is sold under Philips North America.
Look for the specific serial numbers listed in the recall notice.
The recall states there is a potential safety issue that could harm patients during scans, but the exact risk is not clearly described.
Check for the serial numbers 69, 82, 143, 64, 77, 87, 76, 81, 134, 124, 141, 103, 135, 138, 73, 72, 131 on the device.
The recall does not specify a remedy, so contact Philips directly for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0542-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-0542-2025 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.
