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Biomerieux Inc recalls Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalac
Recalled January 6, 2016 · FDA recall Z-0556-2016 · Biomerieux
Hazard
FDA has determined that the product requires 510(k) clearance to continue marketing/distribution in the United States. · FDA Class II
Units
24 cartons
Sold at
US Distribution to states of: CA, GA, IN, MA, MN, MO, NY, OH and PA.
Description
FDA has determined that the product requires 510(k) clearance to continue marketing/distribution in the United States.
Product
Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalactiae in pregnant women using clinical specimens.
Manufacturer(s)
Biomerieux Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →