Events

Recall of Device Recall Centurion Medical Products

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Centurion Medical Products.

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
    56391
  • Event Risk Class
    Class 2
  • Event Number
    Z-1083-2011
  • Event Initiated Date
    2010-06-02
  • Event Date Posted
    2011-02-09
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2011-02-09
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=93882
  • 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
    Custom PICC insertion tray - Product Code LRS
  • Reason
    The kits contain heparin lock flush solution usp code 504505 that is under recall by app pharmaceuticals. app pharmaceuticals is recalling the heparin because of incomplete documentation associated with test results.
  • Action
    Centurion Medical Products sent out Urgent Product Recall Notices on 6/3/2010. A second recall notice was sent to nonresponding consignees on 6/21/2010. The letter instructed the consignees to quarantine the recalled product and contact Centurion so that the recalled product can be retrieved.

Device

Device Recall Centurion Medical Products

Manufacturer

Centurion Medical Products
  • Manufacturer Address
    Centurion Medical Products, 301 Catrell Dr, Howell MI 48843-1703
  • Manufacturer Parent Company (2017)
    Medline Industries Inc.
  • Source
    USFDA