Philips recalls SmartPath to dStream 3.0T MRI coils with model 782145 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 3.0T MRI coils with model number 782145 because the coil's seal adhesive might fail, creating sharp edges that could cause skin injuries like cuts, bruises, or hair loss during scans. Patients using these coils should stop using them immediately to avoid potential harm.
The adhesive in the coil's seal 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 scanning.
Patients using the recalled SmartPath to dStream 3.0T MRI coils with model number 782145 are at risk. Medical staff operating these devices may also be affected if the coils are used improperly.
Check for the model number 782145 on the SmartPath to dStream 3.0T MRI coil. The recall covers all units with this specific model number, as no serial numbers are listed.
Immediately stop using the recalled SmartPath to dStream 3.0T MRI coil with model number 782145 to prevent potential skin injuries.
The recall record does not mention any remedy or fix for this issue.
Check for the model number 782145 on the SmartPath to dStream 3.0T MRI coil. The recall covers all units with this specific model number.
The recall states that the faulty adhesive could cause skin abrasions, bruises, lacerations, hair loss, entanglement, or tissue injury during scans.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1783-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1783-2025 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.
