Granada Biphasic Broth The product is a selective recall
Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalactiae in pregnant women using…
Why was Granada Biphasic Broth The product is a selective recalled?
FDA has determined that the product requires 510(k) clearance to continue marketing/distribution in the United States.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
REF 42722 - Lot Numbers 896, 897 & 899
- Product
- Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalactiae in pregnant women using…
- Recalling firm
- Biomerieux Inc
- Quantity
- 24 cartons
- Distribution
- US Distribution to states of: CA, GA, IN, MA, MN, MO, NY, OH and PA.
- Recall date
- January 6, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)