Events

Recall of Device Recall Interpore Cross International

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Interpore Cross International 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
    27724
  • Event Risk Class
    Class 2
  • Event Number
    Z-0211-04
  • Event Initiated Date
    2003-11-07
  • Event Date Posted
    2003-12-11
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2004-04-20
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30412
  • 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
    Antiserum, Digoxin - Product Code DKA
  • Reason
    Step drills from lot 25947 may have been mis-etched.
  • Action
    The consignees will be notified by letter.

Device

Device Recall Interpore Cross International

Manufacturer

Interpore Cross International Inc
  • Manufacturer Address
    Interpore Cross International Inc, 181 Technology Dr, Irvine CA 92618-2402
  • Source
    USFDA