Philips recalls Achieva XR MRI scanners with model numbers 781153 and 781253 due to potential sharp edges from failing coil seal adhesive, which may 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 two specific models of Achieva XR MRI scanners because the coil seal adhesive might fail, creating sharp edges that could cause skin injuries like cuts, bruises, or tissue damage during scans. This risk affects patients who undergo MRI procedures with these machines.
The QBC seal adhesive in the scanner may weaken over time, causing the seal to become loose during MRI scans. This can create sharp edges that contact patients' skin, potentially leading to abrasions, lacerations, or tissue injury.
Patients using Philips Achieva XR MRI scanners with model numbers 781153 or 781253 are at risk during scans. Healthcare providers who operate these machines should monitor for potential seal failures.
Check the model number on your Philips Achieva XR scanner. Affected units have model numbers 781153 or 781253. All units with these model numbers are included in the recall.
Look for the model number on your scanner's label to confirm if it is 781153 or 781253.
Reach out to Philips North America directly for guidance on next steps if your scanner is affected.
Model numbers 781153 and 781253 are affected.
Yes, if the QBC seal becomes loose during scanning, it may cause skin abrasions, lacerations, or tissue injury.
Check the model number on your scanner's label; affected units have model numbers 781153 or 781253.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0949-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0949-2024 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.
