Ameditech Inc: Medical Device Recall in 2019 - (Recall #: Z-0692-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

QuickTox 5 Panel Drug Screen DipCard

Product Classification:

Class III

Date Initiated: February 15, 2019

Date Posted: December 25, 2019

Recall Number: Z-0692-2020

Event ID: 84239

Reason for Recall:

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)

Status: Terminated

Product Quantity: 3400 units (136 kits)

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

Voluntary or Mandated:

Voluntary: Firm initiated