FDAJanuary 3, 2024device

Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

0088483806844500884838068438

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →
Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261. — Recall Details · AllClear