Exactech, Inc. Optetrak, B-series cemented finned tibial tray size 2f/2t. Catalog # 220-04-02 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Optetrak, B-series cemented finned tibial tray size 2f/2t. Catalog # 220-04-02
Brand
Exactech, Inc.
Lot Codes / Batch Numbers
Serial numbers 0886395-0886424
Products Sold
Serial numbers 0886395-0886424
Exactech, Inc. is recalling Optetrak, B-series cemented finned tibial tray size 2f/2t. Catalog # 220-04-02 due to Improperly machined parts: The Cemented Finned Tibial Trays could not seat the size 2 mating trial or polyethylene insert.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Improperly machined parts: The Cemented Finned Tibial Trays could not seat the size 2 mating trial or polyethylene insert.
Recommended Action
Per FDA guidance
The recall was initiated on August 31, 2006. The distributors were notified by FAX, email and telephone. The returned devices will be stored quarantine.
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