Philips recalls Intera 0.5T Standard MRI machines with model 781101 due to potential sharp edges from a failing coil seal that could cause skin injuries 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 0.5T Standard MRI machines with model number 781101 because the coil seal adhesive might fail, creating sharp edges that could cause skin injuries like cuts, bruises, or hair loss during scans. This is a safety issue that requires immediate attention to prevent harm to patients.
The Quadrature Body Coil (QBC) seal adhesive may fail during MRI scans, creating sharp edges that can contact patients. This could lead to skin abrasions, bruises, lacerations, hair loss, or tissue injury if the seal becomes loose during the scanning process.
Patients using the Intera 0.5T Standard MRI machine with model number 781101 are at risk. Medical facilities that operate this model should check if they have affected units.
Check for the model number 781101 on the Intera 0.5T Standard MRI machine. The recall covers all units with this specific model number, regardless of serial numbers.
Inspect the Quadrature Body Coil (QBC) seal for signs of sharp edges or looseness before use.
The recall does not specify if patients currently in scans are affected. The hazard is potential for injury during future scans if the seal fails.
Check the model number on your Intera 0.5T Standard MRI machine; the recalled model is 781101.
The recall does not provide specific instructions for this scenario. Contact Philips for further guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1771-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1771-2025 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.
