Philips recalls Mammotrak Interventional Coil 3.0T 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 its Mammotrak Interventional Coil 3.0T for potential patient harm during scans. This recall affects specific models with listed serial numbers, and users should check if their device is included.
The recall states a potential safety issue where a patient could be harmed while preparing for or during a scan. However, the exact mechanism of harm is not specified in the record.
Patients undergoing MRI scans with the recalled coil may be at risk. Medical professionals using the device for scans are also affected.
Check if your Mammotrak Interventional Coil 3.0T has serial numbers 73, 96, 58, 95, 119, 26, 16, 56, 94, 38, 28, 66, 135, 120, 2, or 76. The device is sold by Philips North America.
Verify if your Mammotrak Interventional Coil 3.0T has the listed serial numbers: 73, 96, 58, 95, 119, 26, 16, 56, 94, 38, 28, 66, 135, 120, 2, or 76.
The recall states a potential safety issue where a patient may be harmed during scans, but the exact risk level is not specified in the record.
Check if your Mammotrak Interventional Coil 3.0T has serial numbers 73, 96, 58, 95, 119, 26, 16, 56, 94, 38, 28, 66, 135, 120, 2, or 76.
The recall record does not specify a remedy, so contact Philips directly for instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0544-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-0544-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
