Biomet, Inc. Biomet Interlok 67 mm Fixed Cruciate Tibial Plate with Locking Bar; CO-CR-MO/TI 6AL 4V Alloy; Product Number/REF 141232, Biomet Orthopedics, Inc., Warsaw, IN 46582 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Biomet Interlok 67 mm Fixed Cruciate Tibial Plate with Locking Bar; CO-CR-MO/TI 6AL 4V Alloy; Product Number/REF 141232, Biomet Orthopedics, Inc., Warsaw, IN 46582
Brand
Biomet, Inc.
Lot Codes / Batch Numbers
Lot 626520.
Products Sold
Lot 626520.
Biomet, Inc. is recalling Biomet Interlok 67 mm Fixed Cruciate Tibial Plate with Locking Bar; CO-CR-MO/TI 6AL 4V Alloy; Produ due to Mislabeled as to size: the package actaully contained a 71 mm tray.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Mislabeled as to size: the package actaully contained a 71 mm tray.
Recommended Action
Per FDA guidance
Consignees were notified via letter dated 9/18/07 to discontinue use of the product and to return it to the firm.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026