Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
FilmArray BCID Panel (Blood Culture Identification Panel) Recalled by BioFire Diagnostics, LLC Due to There is an increased risk of false positive...
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 BioFire Diagnostics, LLC directly.
Affected Products
FilmArray BCID Panel (Blood Culture Identification Panel), Catalog numbers RFIT-ASY-0126 (30 test kit) and RFIT-ASY-0127 (6 test kit), when used with all lots of BD BACTEC Blood Culture Bottles, Catalog numbers 442020, 442021, 442023, 442192, 442265, 442194, 442022, 442193, 442260, and 442191.
Quantity: N/A
Why Was This Recalled?
There is an increased risk of false positive Proteus results when the product is used with specific types of BD BACTEC blood culture bottles.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About BioFire Diagnostics, LLC
BioFire Diagnostics, LLC has 40 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report