Skip to content
Recall Observatory FDA recall evidence

Device product

QuickTox 5 Panel Drug Screen DipCard

Z-0692-2020

February 15, 2019

Class III

Product summary

Firm
Ameditech Inc
Event
Event 84239
Status
Terminated
Classification
Class III
Quantity
3400 units (136 kits)
Official record key
device-enforcement:Z-0692-2020

Official wording

Reason: 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)

Code information: Catalog Number: QT11 Lot Number: 188787

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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)