Events

Recall of VISION SALMONELLA AGGLUTINATING ANTISERUM GROUP E3 FACTOR 34

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by PRO-LAB DIAGNOSTICS.

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
    125160
  • Event Risk Class
    III
  • Event Initiated Date
    2006-04-05
  • 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
    The titer of the antiserum could no longer be detected indicating that the product was exhibiting instability prior to its expiry date. product is used by clinical lab for serological identification of organis.

Device

VISION SALMONELLA AGGLUTINATING ANTISERUM GROUP E3 FACTOR 34
  • Model / Serial
    Model Catalog: (Lot serial: )
  • Product Description
    vision salmonella agglutinating anti..
  • Manufacturer
    PRO-LAB DIAGNOSTICS

Manufacturer

PRO-LAB DIAGNOSTICS