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FDAJuly 1, 2019device

Universal Sexual Health Testing Kit

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

The hazard

A supplier informed PrivaPath Diagnostics that there is a potential for damaged tubes which could result in blood exposure or erroneous results due to an inappropriate blood-to-additive ratio.

What to do

FDA enforcement status: Terminated

Brands named

privapath diagnosticsprivapath

Recall history

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

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Universal Sexual Health Testing Kit — Recall Details · AllClear