Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Granada Biphasic Broth The product is a selective medium for Recalled by Biomerieux Inc Due to FDA has determined that the product requires 510(k)...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Biomerieux Inc directly.
Affected Products
Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalactiae in pregnant women using clinical specimens.
Quantity: 24 cartons
Why Was This Recalled?
FDA has determined that the product requires 510(k) clearance to continue marketing/distribution in the United States.
Where Was This Sold?
This product was distributed to 9 states: CA, GA, IN, MA, MN, MO, NY, OH, PA
About Biomerieux Inc
Biomerieux Inc has 368 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report