Philips recalls SmartPath to dStream 1.5T MRI coils with model 782146 due to potential sharp edges from adhesive failure causing 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 SmartPath to dStream 1.5T MRI coils with model number 782146 because the coil's 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 adhesive holding the coil's seal may fail during scanning, creating sharp edges that can contact patients' skin. This could lead to cuts, bruises, hair loss, or tissue injury if the seal becomes loose.
Patients undergoing MRI scans with the recalled SmartPath to dStream 1.5T coil model 782146 are at risk. Medical staff using the device should also be cautious during scans.
Check for the model number 782146 on the SmartPath to dStream 1.5T MRI coil. The product was sold with all serial numbers and model number 782146.
Verify the model number on the SmartPath to dStream 1.5T MRI coil; the recalled model is 782146.
Reach out to Philips customer support for guidance on next steps if you have the recalled model.
The recalled model number is 782146.
The official recall does not specify if the coil can be used safely after the recall; contact Philips for guidance.
The recall states the risk includes skin abrasions, bruises, lacerations, hair loss, entanglement, and tissue injury.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1782-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1782-2025 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.
