Philips recalls Intera 1.5T Omni/Stellar MRI scanners (model 781104) due to potential sharp edges from a failing coil seal adhesive, which may 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 Intera 1.5T Omni/Stellar MRI scanners with model number 781104 because the coil seal adhesive might fail, creating sharp edges that could injure patients during scans. This risk is serious enough to require immediate action to prevent skin injuries.
The Quadrature Body Coil (QBC) seal adhesive may fail during scans, creating sharp edges that can contact patients. This could lead to skin abrasions, lacerations, bruising, hair loss, or tissue injury if the seal becomes loose.
Patients undergoing MRI scans with the recalled Intera 1.5T Omni/Stellar scanners are at risk. Healthcare providers using these scanners for medical imaging should also take action.
The recalled scanners have model number 781104. They were sold with all serial numbers listed in the recall notice. This model is part of the Intera 1.5T Omni/Stellar MRI series.
Discontinue use of the Intera 1.5T Omni/Stellar MRI scanner with model number 781104 until further instructions are received.
This recall applies to Philips Intera 1.5T Omni/Stellar MRI scanners with model number 781104. Check your scanner's model number to see if it is affected.
If the Quadrature Body Coil (QBC) seal adhesive fails, it may create sharp edges that could cause skin abrasions, lacerations, bruising, hair loss, or tissue injury during scans.
The recalled model is 781104. Check your scanner's model number and compare it to the list provided in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1777-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1777-2025 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.
