Events

Recall of DrugCheck 3 Test Cup COC/MET/THC || Product Code 60300

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Drug Free Enterprises Inc.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    27074
  • Event Risk Class
    Class 3
  • Event Number
    Z-1245-03
  • Event Initiated Date
    2003-03-20
  • Event Date Posted
    2003-09-23
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2003-09-22
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=29133
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Enzyme Immunoassay, Cocaine And Cocaine Metabolites - Product Code DIO
  • Reason
    Label lacks professional use legend and name and address of the manufacturer.
  • Action
    The firm sent a letter to customers requesting that they overlabel their stock on 3/20/2003. This recall is complete.

Device

DrugCheck 3 Test Cup COC/MET/THC || Product Code 60300

Manufacturer

Drug Free Enterprises Inc
  • Manufacturer Address
    Drug Free Enterprises Inc, 5302 Derry Ave., Ste A, Agoura Hills CA 91301
  • Source
    USFDA