FDAJune 12, 2015device
GE Healthcare Precision RXi 23A/32A Analog System
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.
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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