FDAAugust 7, 2015device

CARESTREAM DRX-EVOLUTION X-Ray System Product Usage: The device is a permanently installed diagnostic X-ray system for general radiographic x-ray imaging including tomography. The tomography feature is not to be used for imaging pediatric patients.

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

The hazard

Software defect that impacts image alignment when using the automatic stitching option for long length images. The defect could cause stitching inconsistencies which may go undetected on a radiograph.

What to do

FDA enforcement status: Terminated

Brands named

carestream healthcarestream

Recall history

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

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CARESTREAM DRX-EVOLUTION X-Ray System Product Usage: The device is a permanently installed diagnostic X-ray system for general radiographic x-ray imaging including tomography. The tomography feature is not to be used for imaging pediatric patients. — Recall Details · AllClear