Recall of Device Recall PTS Panels Lipids Panel test strips

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Polymer Technology Systems, 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
    53773
  • Event Risk Class
    Class 2
  • Event Number
    Z-1136-2010
  • Event Initiated Date
    2009-06-05
  • Event Date Posted
    2010-03-15
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2010-10-20
  • 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
    in vitro diagnostic - Product Code CHH
  • Reason
    Exhibits under-recovery of all analytes.
  • Action
    Consignees were notified by letter dated 6/5/09, advised of the problem, and that the firm would replace product.

Device

  • Model / Serial
    Lot P814; exp. 9/2/09.
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide and international.
  • Product Description
    PTS Panels Lipids Panel test strips for self-testing or professional use with CardioChek P-A analyzers, Manufactured by Polymer Technology Systems, Inc. Catalog # 1710.
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Polymer Technology Systems, Inc., 7736 Zionsville Rd, Indianapolis IN 46268-2175
  • Manufacturer Parent Company (2017)
  • Source
    USFDA