Philips recalls Intera 1.0T Power/Pulsar MRI systems with model 781103 due to potential sharp edges from coil seal adhesive 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 1.0T Power/Pulsar MRI systems with model number 781103 because the coil seal adhesive might fail, creating sharp edges that could injure patients during scans. This risk includes skin abrasions, bruises, lacerations, hair loss, and tissue damage.
The Quadrature Body Coil seal adhesive can fail during MRI scans, creating sharp edges that may contact patients. This could lead to skin abrasions, bruises, lacerations, hair loss, entanglement, or tissue injury.
Patients undergoing MRI scans with the recalled Intera 1.0T Power/Pulsar systems are at risk. Healthcare facilities using these systems for medical imaging may need to take action.
Check for the model number 781103 on the Intera 1.0T Power/Pulsar MRI system. The recall covers all units with this specific model number.
Verify the model number on your Intera 1.0T Power/Pulsar MRI system; the recalled model is 781103.
Reach out to Philips customer support for guidance on next steps for the recalled model.
Yes, patients undergoing MRI scans with the recalled Intera 1.0T Power/Pulsar systems could experience skin injuries from sharp edges created by the coil seal adhesive.
Check for the model number 781103 on your Intera 1.0T Power/Pulsar MRI system; this specific model is recalled.
Contact Philips customer support for guidance on next steps for the recalled model.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1773-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1773-2025 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.
