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Luminex Corporation recalls VERIGENE Processor SP Model No. 10-0000-07. An in vitro diagnostic device intended for processing and identifying nucl
Recalled October 14, 2020 · FDA recall Z-0054-2021 · Luminex
Hazard
No results/incorrect results due to failure of the hybridization heater. · FDA Class II
Units
1 system
Sold at
US distribution in MO. No OUS
Description
No results/incorrect results due to failure of the hybridization heater.
Product
VERIGENE Processor SP Model No. 10-0000-07. An in vitro diagnostic device intended for processing and identifying nucleic acids
Manufacturer(s)
Luminex Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →