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Biomerieux Inc recalls PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculati
Recalled October 17, 2012 · FDA recall Z-0023-2013 · Biomerieux
Hazard
The instrument may not dispense the specimen onto the pre-poured media resulting in a false negative result. · FDA Class II
Units
350 systems
Sold at
Worldwide Distribution-USA (nationwide)-including DC and the states of CA, CO, CT, FL, GA, IL, IN, KY, LA, MO, NC, NJ, NY, OH, OR, PA, RI, SC, TX, and WI, and the country of Canada.
Description
The instrument may not dispense the specimen onto the pre-poured media resulting in a false negative result.
Product
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.
Manufacturer(s)
Biomerieux Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →