Events

Recall of Device Recall Bindazyme

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

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
    26433
  • Event Risk Class
    Class 3
  • Event Number
    Z-0950-03
  • Event Initiated Date
    2003-03-27
  • Event Date Posted
    2003-06-21
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2004-12-01
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=27673
  • 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
    System, Test, Anticardiolipin Immunological - Product Code MID
  • Reason
    Risk of false positives.
  • Action
    Recall notice was sent by fax March 27, 2003. The recall is complete.

Device

Device Recall Bindazyme

Manufacturer

Binding Site Inc The
  • Manufacturer Address
    Binding Site Inc The, 5889 Oberlin Drive 101, San Diego CA 92121
  • Source
    USFDA