FDAJune 10, 2021device

OEC Elite mobile C-arm - Product Usage: intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/devices, and contrast agents during diagnostic, interventional, and surgical procedures.

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

The hazard

There is a potential that the coin cell battery used to monitor X-Ray tube temperature may deplete early causing the system to become inoperable.

What to do

FDA enforcement status: Terminated

Brands named

ge oec medical systems

Recall history

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

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