Events

Recall of Device Recall DiaSorin ETIEAG assay 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
    30953
  • Event Risk Class
    Class 3
  • Event Number
    Z-0658-05
  • Event Initiated Date
    2004-11-01
  • Event Date Posted
    2005-03-29
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2006-07-22
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=36883
  • 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
    Epstein-Barr Virus, Other - Product Code LSE
  • Reason
    The diasorin eti-ea-g kits contained the wrong microtiter plate. the plate provided in the kits was for a different product, the protrac ii tacrolimus kit.
  • Action
    Customers were notified of the product and problem via telephone and instructed to check any remaining inventory and discard all incorrect plates. Replacement plates were offered.

Device

Device Recall DiaSorin ETIEAG assay kit
  • Model / Serial
    catalog no. 7570, Lot # 113963C
  • Product Classification
    Immunology and Microbiology Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    FL, TX & UT
  • Product Description
    DiaSorin ETI-EA-G assay kit Catalog No. 7570, lot # 113963C
  • Manufacturer
    Diasorin Inc.

Manufacturer

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