Vanguard PS Open Box Femoral 70 MM Left Interlock, " FOR CEMENTED USE ONLY" CO-CR-MO ALLOY. Biomet, Inc. A knee joint replacement prosthesis non-coated femoral indicated for cemented application only.
Hazard
The recalled device was manufactured with two distal pegs but package labeling indicates the device is pegless.
What You Should Do
Remedy
Biomet Orthopedics sent an "URGENT MEDICAL DEVICE RECALL NOTICE" letter to all affected customers. The letter included: reason for the recall, risks associated with use of the device, and alternate instructions for use of the recalled device. Customers are instructed to quarantine and return the devices, and a return form. For information or questions on this recall call Biomet at (574) 371-3756.
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Products
Vanguard PS Open Box Femoral 70 MM Left Interlock, " FOR CEMENTED USE ONLY" CO-CR-MO ALLOY.
Biomet, Inc.
A knee joint replacement prosthesis non-coated femoral indicated for cemented application onl
- Brand
- Biomet, Inc.
- UPC
- Part # 183132. Lot # 947480.
Units Affected
8