Philips recalls Achieva 1.5T Initial MRI systems with model 781178 due to potential sharp edges from adhesive failure that 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 Achieva 1.5T Initial MRI systems with model number 781178 because the QBC seal adhesive might fail, creating sharp edges that could injure patients during scans. This risk involves skin abrasions, bruises, lacerations, or hair loss. Affected units are being identified for repair or replacement.
The QBC seal adhesive in the MRI system may fail during scanning, 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 undergoing MRI scans with the affected Achieva 1.5T Initial systems are at risk. Healthcare providers using these systems for medical imaging should also be aware of the potential hazard.
Check for model number 781178 on the Achieva 1.5T Initial MRI system. All units with this model number are affected, including those sold under model 781346.
Identify the model number on your Achieva 1.5T Initial system; affected units have model 781178 or 781346.
Reach out to Philips North America for guidance on next steps for affected units.
Check the model number on your Achieva 1.5T Initial system; affected units have model 781178 or 781346.
The QBC seal adhesive may create sharp edges that could cause skin abrasions, bruises, lacerations, hair loss, or tissue injury during scans.
Contact Philips North America directly for instructions on repair or replacement.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0947-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0947-2024 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.
