Stryker Howmedica Osteonics Corp. Osteonics Scorpio Total Knee; Posteriorly Stabilized Femoral Component; #13 with posts, low friction Ion treatment. Use only with Scorpio Posteriorly Stabilized Tibial Bearing Components with Scorpio Patellar Components. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Osteonics Scorpio Total Knee; Posteriorly Stabilized Femoral Component; #13 with posts, low friction Ion treatment. Use only with Scorpio Posteriorly Stabilized Tibial Bearing Components with Scorpio Patellar Components.
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Catalog No. 711-4513L, Lot Code: K04S174
Products Sold
Catalog No. 711-4513L; Lot Code: K04S174
Stryker Howmedica Osteonics Corp. is recalling Osteonics Scorpio Total Knee; Posteriorly Stabilized Femoral Component; #13 with posts, low frictio due to Scorpio Posterior Stabilized Femoral Component labeled and laser marked as a Left, was in fact a Right component.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Scorpio Posterior Stabilized Femoral Component labeled and laser marked as a Left, was in fact a Right component.
Recommended Action
Per FDA guidance
The International Stryker Distributor was notified via an advisory notice with return receipt on March 18, 2005
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