Ameditech Inc recalls QuickTox 5 Panel Drug Screen DipCard

Recall date

February 15, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0692-2020

FDA classification

Class III

Brand / firm

Ameditech Inc

Sold / distributed

US - AZ, CA, FL, GA, KS, LA, MI, MO, MS, NC, OK, TN, and TX. OUS - None

Why it was recalled

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)

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

QuickTox 5 Panel Drug Screen DipCard