Philips recalls Intera 1.5T MRI scanners with model numbers 781195 and 781295 due to potential sharp edges from a failing coil seal that could cause skin injuries during scans.
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.
Philips is recalling specific Intera 1.5T MRI scanners with model numbers 781195 and 781295 because the coil seal adhesive might fail, creating sharp edges that could cause skin injuries like cuts, bruises, or hair loss during scans. This is a safety issue that requires attention to prevent harm to patients.
The QBC seal adhesive in the scanner's coil might fail during use, creating sharp edges. If the seal becomes loose while scanning, these edges could contact patients and cause skin injuries such as cuts, bruises, or hair loss.
Patients using these specific Philips Intera 1.5T MRI scanners with model numbers 781195 or 781295 are at risk. Medical facilities that own these models should check if they have the affected units.
Check for model numbers 781195 or 781295 on the scanner. These units were sold with specific serial numbers and are part of the Philips Intera 1.5T MRI system.
Look for model numbers 781195 or 781295 on the scanner's label or documentation.
Reach out to Philips customer support for guidance on whether your scanner is affected and next steps.
Model numbers 781195 and 781295 are affected.
Yes, the failing seal could cause skin injuries like cuts, bruises, or hair loss during scans.
No, but you should check if your scanner is affected and contact Philips 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-1774-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1774-2025 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.
