Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more Recalled by bioMerieux, Inc. Due to False resistant results for Streptococcus anginosus and Streptococcus...
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
VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more of these susceptibility products: Catalog # 410028, VITEK 2 AST-ST01 Catalog # 420915, VITEK 2 AST-ST02 Catalog # 421040, VITEK 2 AST-ST03 The VITEK 2 Streptococcus Susceptibility Card is intended for use with the VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of S. pneumoniae, beta-hemolytic Streptococcus, and Viridans Streptococcus to antimicrobial agents when used as instructed.
Quantity: 184,374
Why Was This Recalled?
False resistant results for Streptococcus anginosus and Streptococcus constellatus strains were reported.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About bioMerieux, Inc.
bioMerieux, Inc. has 53 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report