Biomet, Inc. Biomet CC Cruciate Tibial Tray, 67 mm.; Product No. 141232, Biomet, Inc., Warsaw, IN 46581 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Biomet CC Cruciate Tibial Tray, 67 mm.; Product No. 141232, Biomet, Inc., Warsaw, IN 46581
Brand
Biomet, Inc.
Lot Codes / Batch Numbers
Lot Number: 448530.
Products Sold
Lot Number: 448530.
Biomet, Inc. is recalling Biomet CC Cruciate Tibial Tray, 67 mm.; Product No. 141232, Biomet, Inc., Warsaw, IN 46581 due to Mislabeled as to size: Package labeled as containing a 67 mm tray actually contains a 75 mm tray and vice versa.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Mislabeled as to size: Package labeled as containing a 67 mm tray actually contains a 75 mm tray and vice versa.
Recommended Action
Per FDA guidance
Consignees were notified via an Urgent Medical Device Recall Notice dated 12/12/07 to cease use of the product and to return it.
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 noticeDistribution
As reported by FDA
GA, ID, IN, MO, OH, VA
Page updated: Jan 10, 2026