Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VITEK¿ 2 Systems Software Version 9.01 Update Kit. Recalled by bioMerieux, Inc. Due to The VITEK¿ 2 Systems Software Version 9.01 software...
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 Systems Software Version 9.01 Update Kit.
Quantity: five (5) VITEK¿ 2 Systems Software version 9.01
Why Was This Recalled?
The VITEK¿ 2 Systems Software Version 9.01 software may display incorrect organism identification information as well as the associated Antimicrobial Susceptibility Testing (AST) results when using the VITEK¿ 2 FLEXPREP" feature.
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