Recall of MINI PLASTICS SET

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-1081-2018
  • 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 contains a pvp prep pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
  • 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
    75700  Lot codes: 2015102790 2016011590 2016030790 2016050490 2016062390 2016071590 2016081790 2016111890 2017012090 2017020790 2017042090
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationally
  • Product Description
    MINI PLASTICS SET
  • Manufacturer

Manufacturer

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