Philips recalls Intera 1.0T Omni/Stellar MRI scanners with model 781102 due to potential sharp edges from adhesive failure that could cause skin abrasions, bruises, or lacerations 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 Intera 1.0T Omni/Stellar MRI scanners with model number 781102 because the QBC seal adhesive might fail, creating sharp edges that could injure patients during scans. This recall matters because patients might experience skin abrasions, bruises, lacerations, or other injuries if the seal becomes loose during scanning.
The QBC seal adhesive in the scanner may fail during use, creating sharp edges that can contact patients. If the seal becomes loose while scanning, it could cause skin abrasions, bruises, lacerations, hair loss, entanglement, or tissue injury.
Patients undergoing MRI scans with the recalled Intera 1.0T Omni/Stellar scanners are at risk. Healthcare facilities using these specific models should be most concerned.
Check for the model number 781102 on the scanner. The recall includes all units with this specific model number sold by Philips Medical Systems Netherlands B.V.
Identify the model number on your Intera 1.0T Omni/Stellar scanner to confirm if it is 781102.
Yes, the QBC seal adhesive may fail, creating sharp edges that could cause skin abrasions, bruises, lacerations, hair loss, entanglement, or tissue injury during scans.
The recall does not specify a remedy, so contact Philips Medical Systems Netherlands B.V. for further instructions.
Check for the model number 781102 on your Intera 1.0T Omni/Stellar scanner.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1772-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1772-2025 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.
