Philips recalls ST SENSE Breast Coil devices with specific serial numbers due to potential safety risks during medical imaging procedures. Affected units may cause patient harm during scans; contact Philips for details.
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Philips is recalling certain ST SENSE Breast Coil devices that could pose a safety risk during medical scans. This recall is important because patients might be harmed while preparing for or undergoing the procedure.
The device may cause harm during medical scans due to a potential safety issue. This could lead to patient injury if the device is used improperly or during the scanning process.
Patients using the recalled breast coil devices for medical imaging are most at risk. The recall affects individuals who have the specific serial numbers listed in the official notice.
Check the serial number on your ST SENSE Breast Coil device. The affected units have specific serial numbers listed in the recall notice, including 36577, 36597, and other numbers provided in the official record.
Look for the serial number on your device to confirm if it is affected by this recall.
Reach out to Philips directly for further instructions on how to address the issue.
Philips recalls these breast coils due to a potential safety issue that could harm patients during medical scans.
Check the serial number against the list provided in the recall notice and contact Philips for further instructions.
The recall indicates a potential safety issue that could cause harm during scans, but no specific immediate risk is stated for normal use.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0547-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-0547-2025 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.
