FDADecember 19, 2014device

GE Healthcare Automatic Mobile X-Ray (AMX) Series: Optima XR220 amx

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

The hazard

An issue was identified with the mAs accuracy check performed on the system that could result in inaccuracies in the 10% to 20% range for exposure times longer than 15 msec.

What to do

FDA enforcement status: Terminated

Brands named

ge healthcare

Recall history

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

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