FDA Medical Device · Z-1469-2017

OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems

Class II · Terminated

OEC FlexiView 8800 workstation power cable assembly issue which can result in a loss of imaging functionality due to intermittent power cord failures.

Affected lots / codes — check yours against thisOEC FlexiView 8800 systems that had NEMA 5-15 15 Amp power cords replaced between January 28, 2016 and November 23, 2016.

Recalling firm: GE OEC Medical Systems, Inc, Salt Lake City, UT
Classification: Class II (temporary or reversible harm possible)
Status: Terminated
Quantity: 1
Distribution: One consignee in CA.
Recall initiated: February 21, 2017
Classified: March 14, 2017
Terminated: April 24, 2017
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1469-2017%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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