FDAJanuary 8, 2024device

BD BBL Sensi Disc Cefixime - 5 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231664¿

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or additional adverse diagnostic outcomes, such as a delay in diagnosis, the selection of inappropriate antibiotics, or extended duration of antibiotic exposure and the treatment process.

What to do

FDA enforcement status: Ongoing

Brands named

becton dickinsonbectonbecton dickinson

UPCs

30382902316641

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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