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

Class I - Dangerous

🏥 Medical Devices Recalled: November 23, 2015 Biomerieux Infusion Pumps

What Should You Do?

Check if you have this product:
REF 42722 - Lot Numbers 896, 897 & 899
Do not eat it: Even if it looks and smells fine, do not consume this product.
Throw it away or return it: You can return the product to the store for a full refund.
Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:: Biomerieux Inc
Reason for Recall:: FDA has determined that the product requires 510(k) clearance to continue marketing/distribution in the United States.
Classification:: Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
Status:: terminated

Product Information

Full Description:

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

Product Codes/Lot Numbers:

REF 42722 - Lot Numbers 896, 897 & 899

Distribution:

Distributed in: US, CA, GA, IN, MA, MN, MO, NY, OH, PA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0556-2016

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