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FDAFebruary 15, 2019device

QuickTox 5 Panel Drug Screen DipCard

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

The hazard

Mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11, LOT #188787) and Alere iScreen Drugs of Abuse Dip Test (P/N X11-IS10-22015-DX LOT #188744)

What to do

FDA enforcement status: Terminated

Brands named

ameditech

Recall history

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

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QuickTox 5 Panel Drug Screen DipCard — Recall Details · AllClear