Philips recalls Intera 3.0T Quasar Dual MRI scanners with model 781150 due to potential sharp edges from failing seal adhesive, which could cause skin abrasions, lacerations, or tissue injury 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 MRI scanners with model number 781150 because the seal adhesive on the Quadrature Body Coil might fail, creating sharp edges that could injure patients during scans. This risk affects patients undergoing MRI procedures with these specific scanners.
The seal adhesive on the Quadrature Body Coil (QBC) may fail during MRI scans, creating sharp edges. These edges could contact patients and cause skin abrasions, lacerations, bruises, hair loss, entanglement, or tissue injury.
Patients using Philips Intera 3.0T Quasar Dual MRI scanners with model number 781150 are at risk. Healthcare facilities that operate these scanners should be aware of the potential for patient injuries during scans.
Check for the model number 781150 on the scanner. The recall covers all units with this specific model number, as no serial numbers are listed in the recall notice.
Verify the model number on the scanner; the recalled units have model number 781150.
The seal adhesive on the Quadrature Body Coil may fail, creating sharp edges that could cause skin abrasions, lacerations, or tissue injury during scans.
The recalled units have model number 781150; check the scanner's label for this specific model number.
The recall does not specify a remedy, so contact Philips directly for guidance on next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1780-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1780-2025 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.
