Reported Jan 6, 2016 · Terminated

Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus…

Biomerieux Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Biomerieux Inc · 595 Anglum Rd · Hazelwood, MO · 63042-2320

Is this the product you have?

  • Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalactiae in pregnant women using clinical specimens.
Lot codes and dates
    • REF 42722 - Lot Numbers 896
    • 897 & 899
Amount recalled
24 cartons

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 24, 2016 · Data as of Sep 19, 6:46 PM UTC

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