Philips recalls Intera 1.5T Explorer/Nova Dual MRI scanners with model 781108 due to potential sharp edges from failing QBC seal adhesive, which could cause skin abrasions 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 certain Intera 1.5T MRI scanners that may have a seal adhesive issue causing sharp edges. This could lead to skin injuries like cuts, bruises, or hair loss during scans if the seal becomes loose.
The QBC seal adhesive in the scanner may fail during use, creating sharp edges that can contact patients. This could result in skin abrasions, lacerations, bruising, hair loss, or tissue injury if the seal becomes loose during the scanning process.
Patients undergoing MRI scans with the recalled Intera 1.5T Explorer/Nova Dual scanners are at risk. Healthcare providers using these scanners for medical imaging should also be aware.
Check for the model number 781108 on the scanner. The recall applies to all units with this specific model number, regardless of serial number.
Look for the model number 781108 on the scanner to confirm if it is affected.
Yes, patients using the recalled Intera 1.5T Explorer/Nova Dual scanners may experience skin injuries if the QBC seal becomes loose during scanning.
Check for the model number 781108 on the scanner. The recall applies to all units with this specific model number.
The recall does not specify a remedy, so contact Philips directly for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1775-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1775-2025 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.
