Device Recall Biomet Orthopedics DCM AGC Molded Tibial Component

  • Model / Serial
    Lot 311500; exp. 2012-02.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Class II Recall - Worldwide Distribution --- USA including states of IA, SD, and countries of Brazil and Chile.
  • Product Description
    Biomet --DCM AGC Molded Tibial Implant (12 mm x 80 mm)--Biomet Orthopedics , Interlok finish/posterior stabilized, 12 mm thick x 80 mm wide, UHMWPE/CO-CR-MO alloy, sterile; REF 155364, Biomet Orthopedic, Inc.
  • Manufacturer
  • 1 Event

Manufacturer

  • 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

  • Model / Serial
    Lot 918930; exp. 2012-02.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Class II Recall - Worldwide Distribution --- USA including states of IA, SD, and countries of Brazil and Chile.
  • Product Description
    Biomet Orthopedics DCM AGC Molded Tibial Component, 12 mm thick x 80 mm, UHMWPE/CO-CR-MO alloy, sterile; REF 155116.
  • Manufacturer