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GE OEC Medical Systems, Inc recalls OEC 9800. MDL Numbers: D222250, D141598
Recalled February 1, 2017 · FDA recall Z-1059-2017 · GE OEC Medical Systems
Hazard
GE Healthcare Surgery announces a voluntary field action for the OEC 9800 and OEC 9900 Elite due to additional supplementation to the user documentation to include areas for enhanced planned maintenance and component replacement frequencies. · FDA Class II
Units
26,256 total
Sold at
Worldwide including govt/VA/military and foreign consignees.
Description
GE Healthcare Surgery announces a voluntary field action for the OEC 9800 and OEC 9900 Elite due to additional supplementation to the user documentation to include areas for enhanced planned maintenance and component replacement frequencies.
Product
OEC 9800. MDL Numbers: D222250, D141598
Manufacturer(s)
GE OEC Medical Systems, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →