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Device Recall Biomet Orthopedics DCM AGC Molded Tibial Component
Model / Serial
Lot 311500; exp. 2012-02.
Product Classification
Orthopedic Devices
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
Biomet, Inc.
1 Event
Recall of Device Recall Biomet Orthopedics DCM AGC Molded Tibial Component
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Manufacturer
Biomet, Inc.
Manufacturer Address
Biomet, Inc., 56 E Bell Dr, Warsaw IN 46581-0587
Source
USFDA
One device with a similar name
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Device Recall Biomet Orthopedics DCM AGC Molded Tibial Component
Model / Serial
Lot 918930; exp. 2012-02.
Product Classification
Orthopedic Devices
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
Biomet, Inc.
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