Philips recalls Intera 1.5T Achieva Nova MRI scanners with model 781172 due to potential sharp edges from failing coil seal adhesive, which 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 Intera 1.:5T Achieva Nova MRI scanners with model number 781172 because the coil seal adhesive might fail, creating sharp edges that could cause skin injuries like cuts, bruises, or hair loss during scans.
The QBC seal adhesive in the scanner might fail during use, creating sharp edges. These edges could contact patients during scans, leading to skin abrasions, bruises, lacerations, hair loss, or tissue injury.
Patients using the recalled MRI scanners may face risks during scans. Medical staff using these scanners are most at risk due to the potential for injuries during procedures.
Check for the model number 781172 on the scanner. All units affected by this recall were sold by Philips North America.
Look for the model number 781172 on the scanner to confirm if it is affected.
Yes, Philips is recalling Intera 1.5T Achieva Nova MRI scanners with model number 781172.
The QBC seal adhesive may fail, creating sharp edges that could cause skin abrasions, bruises, lacerations, hair loss, or tissue injury during scans.
Check for the model number 781172 on the scanner. All units affected by this recall were sold by Philips North America.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0952-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0952-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
