Recall of Device Recall DiaSorin GammaCoat Androstenedione 125I RIA Kit

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Diasorin 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
    30937
  • Event Risk Class
    Class 3
  • Event Number
    Z-0634-05
  • Event Initiated Date
    2004-07-15
  • Event Date Posted
    2005-03-18
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2006-07-22
  • Event Source
    USFDA
  • Event Source URL
  • 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
    Radioimmunoassay, Androstenedione - Product Code CIZ
  • Reason
    Standards used in the gammacoat androstenedione radioimmunoassay kit appeared yellowish in color and were gelatinous upon reconstitution.
  • Action
    Customers were sent a customer notification letter identifying the product and the problem and requesting a response identifying the number of replacement kits needed.

Device

  • Model / Serial
    Catalog No. CA 1725, Lot # 05144
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    MN, MA, KY, Saudi Arabia, Jordan, Sweden, Germany, Spain, Belgium, Italy, Canada, Australia, Portugal, Hungary, Switzerland & Israel
  • Product Description
    DiaSorin GammaCoat Androstenedione - [125I] RIA Kit Catalog No. CA-1725, DiaSorin Stillwater, Minnesota 55082-0285, U.S.A. Lot # 05144. for the quantitative determination of androstenedione levels in serum.
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Diasorin Inc., 1951 Northwestern Ave S, Stillwater MN 55082-7536
  • Manufacturer Parent Company (2017)
  • Source
    USFDA