FDAOctober 20, 2015device

iCup Drug Screen Cup, Item No. I-DXA-187-016, I-DXA-167-013; iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142; iCup DX 11 Panel w/Adulterant, Item No. I-DXA-1117-131; iCup DX 12 Panel w/Adulterant, Item No. I-DXA-1127-023; iCup DX 6 Panel w/Adulterant, Item No. I-DXA-167-013; iCup DX 8 Pane...

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

The hazard

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

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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