Civco Medical Instruments Co. Inc. recalls VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX
Recalled Product
VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX
Hazard / Issue
There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Part Number 610-1059; UDI 00841436101882 Lot Numbers: A108295, A111466, A111759, A112392, A113288, A113874, A116720, A118295, A118557, A119369, A120039, A120344, A120567, A120641, A120807, A121367, A121506, A121516, A121866, A122103, A123138, A124555, A125980, A127569, A127842, A129198, A129948, A129949, A129950, A130252, A131213, A131428, A132258, A132471, A133741, A133742, A133823, A134199, A134203, A135587, A135846, A136274, A136787, A137788, A138199, A138307, A138805, A139478, A140029, A140660, A142719, A143236, A144157, A144317, A144992, A145774
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