Philips recalls Ingenia 1.5T CX MRI scanners with model numbers 781261 and 781262 due to potential sharp edges from a failing coil seal adhesive, which 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 two specific models of MRI scanners (781261 and 781262) because the coil seal adhesive might fail, creating sharp edges that could cause skin injuries like cuts, bruises, or hair loss during scans.
The QBC seal adhesive in the scanner's coil can fail during use, creating sharp edges that might contact patients. This could lead to skin abrasions, bruises, lacerations, hair loss, or tissue injury during the scanning process.
Patients undergoing MRI scans with these specific Philips Ingenia 1.5T CX scanners are at risk. Healthcare providers using these models for medical imaging may also be affected.
Check for model numbers 781261 or 781262 on the scanner. These units were sold with UDI-DI codes 00884838068438 or 00884838068445.
Look for model numbers 781261 or 781262 on the scanner's label or documentation.
Reach out to Philips North America for guidance on next steps if you have the recalled model.
The QBC seal adhesive may fail, creating sharp edges that could cause skin injuries like cuts, bruises, or hair loss during scans.
Model numbers 781261 and 781262, with UDI-DI codes 00884838068438 and 00884838068445 respectively.
No immediate stop is required, 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-0950-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0950-2024 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.
