Philips recalls SmartPath to dStream 1.5T MRI scanners with model numbers 781260 and 782112 due to potential sharp edges from adhesive failure that could cause skin abrasions or tissue injury 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 specific MRI scanners that may have adhesive failure in the patient coil, risking skin injuries like cuts or bruising during scans. This is serious but only affects the recalled models.
The adhesive holding the patient coil may fail during scans, creating sharp edges that can cause skin injuries like cuts, bruises, or tissue damage. This risk occurs when the coil becomes loose during the scanning process.
Patients undergoing MRI scans with the recalled Philips SmartPath to dStream 1.5T scanners are at risk. Healthcare providers using these models should check if their equipment is affected.
Check for model numbers 781260 or 782112 on the scanner. All units with these models are affected, regardless of when they were purchased.
Look for model numbers 781260 or 782112 on the scanner's label or documentation.
Yes, the adhesive may fail during scans, causing skin injuries like cuts or bruises. However, the risk is not immediate and only affects specific models.
Check for model numbers 781260 or 782112 on the scanner. All units with these models are affected.
The recall does not specify a remedy, so contact Philips directly for guidance on next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0955-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0955-2024 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.
