Philips recalls two models of 1.5T Conversion MRI scanners due to potential sharp edges from failing adhesive in the Quadrature Body Coil, which could cause skin abrasions or lacerations 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 two specific models of 1.5T MRI scanners because the adhesive holding the Quadrature Body Coil might fail, creating sharp edges that could injure patients during scans. This risk requires immediate attention to prevent skin injuries.
The adhesive in the Quadrature Body Coil (QBC) seal may weaken over time, causing the seal to become loose during scans. This can create sharp edges that contact patients, potentially leading to skin abrasions, lacerations, or other injuries.
Patients undergoing MRI scans with the recalled Philips Achieva 1.5T Conversion models (781346 and 781283) are at risk. Medical staff using these scanners may also face injury if the QBC seal fails during procedures.
Check for model numbers 781346 or 781283 on the scanner. The recall includes all units with these specific model numbers, regardless of when they were sold.
Identify the model number on your Philips Achieva 1.5T Conversion scanner to see if it matches 781346 or 781283.
Reach out to Philips North America for guidance on next steps if your scanner is affected.
The adhesive in the Quadrature Body Coil seal may fail, creating sharp edges that could cause skin injuries during MRI scans.
Patients may experience skin abrasions, bruises, lacerations, hair loss, entanglement, or tissue injury if the QBC seal becomes loose during scanning.
Check for model numbers 781346 or 781283 on your Philips Achieva 1.5T Conversion scanner.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0946-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0946-2024 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.
