Events

Recall of INSTACHECK DRUG SCREEN TEST - THC (CANNAKINOIDS)

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by APPLIED BIOTECH 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
    80791
  • Event Risk Class
    III
  • Event Initiated Date
    2005-05-27
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
  • Reason
    Internal audit determined that all instacheck and instacup product lines expect instacheck med+9 panel drug screen with tca did not meet performance expectations.

Device

INSTACHECK DRUG SCREEN TEST - THC (CANNAKINOIDS)
  • Model / Serial
    Model Catalog: 115C (Lot serial: all lots)
  • Product Description
    all InstaCup/InstaCheck products
  • Manufacturer
    APPLIED BIOTECH INC

Manufacturer

APPLIED BIOTECH INC
  • Manufacturer Address
    SAN DIEGO
  • Source
    HC