Philips recalls specific Achieva 1.5T MRI scanners (model numbers 781196, 781343, 781296) due to potential sharp edges from failing coil seals 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 three specific models of 1.5T MRI scanners because their coil seals might fail, creating sharp edges that could cause skin injuries like cuts, bruises, or hair loss during scans. This is a safety issue for patients using these machines.
The QBC seal adhesive in these MRI scanners may fail during 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.
Patients using Philips Achieva 1.5T MRI scanners with model numbers 781196, 781343, or 781296 are at risk. Medical facilities that own these models should check if they have the affected units.
Check the model number on your Philips Achieva 1.5T scanner. Affected models are 781196, 781343, and 781296. All units are affected, so no units are safe without verification.
Identify your scanner's model number to see if it matches 781196, 781343, or 781296.
The QBC seal adhesive may fail, creating sharp edges that could cause skin injuries during scans.
Check your model number to see if it's affected. If yes, contact Philips for guidance.
No, only specific model numbers 781196, 781343, and 781296 are affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0945-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0945-2024 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.
