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FDANovember 21, 2014device

DrugCheck Ketamine Dip Test 31317-3P PRO-EU-SWE, 31226-3-CA-GML, 30842 TR, 30108C, 30108C CAN, 30108C EU, and 30108C INT. This assay provides only a preliminary analytical test result.

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

The hazard

This recall has been initiated due to potential false positives results when using the test to screen for Ketamine. Use of this product may give incorrect screening results.

What to do

FDA enforcement status: Terminated

Brands named

express diagnostics int lexpressexpress diagnostics

Recall history

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

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