Stryker Howmedica Osteonics Corp. Duracon Total Knee Modular Femoral Component; Non-Porous Right Medium Assembly, Product No. 6632-0-325 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Duracon Total Knee Modular Femoral Component; Non-Porous Right Medium Assembly, Product No. 6632-0-325
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Product No. 6632-0-325, Lot code UCVO
Products Sold
Product No. 6632-0-325; Lot code UCVO
Stryker Howmedica Osteonics Corp. is recalling Duracon Total Knee Modular Femoral Component; Non-Porous Right Medium Assembly, Product No. 6632-0-3 due to Loose fixation pegs: One lot of femoral components may have loose fixation pegs.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Loose fixation pegs: One lot of femoral components may have loose fixation pegs.
Recommended Action
Per FDA guidance
Notification letters, dated 10/17/2006, were sent via Federal Express on 10/17/2006 to all consignees requesting return of product.
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, IN
Page updated: Jan 10, 2026