Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Achieva 3.0T. Model. (REF) Numbers 781277 Recalled by Philips North America Due to The Quadrature Body Coil (QBC) seal adhesive may...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips North America directly.
Affected Products
Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345.
Quantity: 75 US; 442 OUS
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America
Philips North America has 107 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report