FDAMarch 29, 2023device

binx io CT/NG Assay- Single-use Cartridge for the qualitative detection of Chlamydia trachomatis and Neisseria gonorrhoeae Ref: 1.002.101

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

The hazard

May not meet the declared performance characteristics for the detection of Chlamydia trachomatis (CT) within the labeled expiry period, potential to produce either false negative CT or positive CT results

What to do

FDA enforcement status: Ongoing

Brands named

binx healthbinx

UPCs

506044176005000210869309

Recall history

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

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binx io CT/NG Assay- Single-use Cartridge for the qualitative detection of Chlamydia trachomatis and Neisseria gonorrhoeae Ref: 1.002.101 — Recall Details · AllClear