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Express Diagnostics Int'l., Inc. recalls DrugCheck Ketamine Dip Test 31317-3P PRO-EU-SWE, 31226-3-CA-GML, 30842 TR, 30108C, 30108C CAN, 30108C EU, and 30108C IN
Recalled February 11, 2015 · FDA recall Z-1033-2015 · Express Diagnostics Int'l
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. · FDA Class II
Units
5,050
Sold at
Worldwide Distribution -- US, including the states of CA, NY, MN, and SC; SWEDEN, CANADA, UNITED KINGDOM, and GUATEMALA.
Description
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.
Product
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.
Manufacturer(s)
Express Diagnostics Int'l., Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →