Recall of PEDIATRIC IV & IV START KIT

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

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
    79329
  • Event Risk Class
    Class 2
  • Event Number
    Z-1092-2018
  • Event Initiated Date
    2017-10-23
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2018-06-21
  • 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
    Tray, surgical - Product Code LRP
  • Reason
    Convenience kit containing components to assist practitioner with iv placement and securement.
  • Action
    On October 16, 2017 a PRODUCT CORRECTION letter was issued to customers notifying them that if they had any kits in their inventory, Centurion will supply labels to affix to the front of each kit instructing the user to discard the prep pad upon opening the kit. Other components of the kit may continue to be used and are NOT within the scope of this recall.

Device

  • Model / Serial
    IV5785 IV6135  Lot codes: 2015121890 2016031490 2016102490 2016111490 2017012390 2017050890 2016071190 2015101990 2015120790 2016010490 2016012590 2016101090 2017010290 2017061990 2017071090
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationally
  • Product Description
    PEDIATRIC IV & IV START KIT
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Centurion Medical Products Corporation, 100 Centurion Way, Williamston MI 48895-9086
  • Manufacturer Parent Company (2017)
  • Source
    USFDA