Philips recalls Intera CV MRI scanners with model 781107 due to potential sharp edges from adhesive failure that 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 Intera CV MRI scanners with model number 781107 because the seal adhesive might fail, creating sharp edges that could injure patients during scans. This risk affects patients undergoing MRI procedures with these specific scanners.
The adhesive in the Quadrature Body Coil (QBC) seal may fail during MRI scans, creating sharp edges. These edges could contact patients and cause skin abrasions, bruises, lacerations, hair loss, entanglement, or tissue injury.
Patients using Philips Intera CV MRI scanners with model number 781107 are at risk. Healthcare facilities that operate these scanners should monitor for potential injuries during scans.
Check for the model number 781107 on the scanner. This recall applies to all units with this specific model number, regardless of serial number or other identifiers.
Verify the model number on your Philips Intera CV scanner to confirm it is 781107.
Reach out to Philips directly for guidance on next steps if you have the recalled model.
Yes, patients using the recalled Intera CV scanners with model 781107 may experience skin injuries from sharp edges created by adhesive failure.
Check for the model number 781107 on your Philips Intera CV scanner. This recall applies to all units with this specific model number.
Contact Philips directly for guidance on next steps if you have the recalled model number 781107.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1781-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1781-2025 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.
