Devices

Device Recall Biomet Graft Preparation System

  • Model / Serial
    Lots 192180, exp. Jan 2012; 223260, exp. Jan 2012 and 652330, exp May 2011.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Chile, Italy, Spain and United Kingdom.
  • Product Description
    Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, Inc., Warsaw, Indiana; REF 800-0300.
  • Manufacturer
    Biomet, Inc.
  • 1 Event

Manufacturer

Biomet, Inc.
  • Manufacturer Address
    Biomet, Inc., 56 E Bell Dr, Warsaw IN 46581-0587
  • Source
    USFDA

One device with a similar name

Learn more about the data here

Device Recall Biomet Graft Preparation System
  • Model / Serial
    Lot 192380, exp. Jan 2012.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Chile, Italy, Spain and United Kingdom.
  • Product Description
    Vortech Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, Inc., Warsaw, Indiana; REF 800-0300V. (Not sold in the United States).
  • Manufacturer
    Biomet, Inc.