FDANovember 23, 2015device

Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalactiae in pregnant women using clinical specimens.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

FDA has determined that the product requires 510(k) clearance to continue marketing/distribution in the United States.

What to do

FDA enforcement status: Terminated

Brands named

biomerieux

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalactiae in pregnant women using clinical specimens. — Recall Details · AllClear