Stryker Howmedica Osteonics Femoral Resection Guide, Scorpio L.R.S. Instrumentation. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Femoral Resection Guide, Scorpio L.R.S. Instrumentation.
Brand
Stryker Howmedica Osteonics
Lot Codes / Batch Numbers
Catalog No: 8050-5103, 8050-5105, 8050-5107, 8050-5109, 8050-5111, 8050-5113.
Products Sold
Catalog No: 8050-5103; 8050-5105; 8050-5107; 8050-5109; 8050-5111; 8050-5113.
Stryker Howmedica Osteonics is recalling Femoral Resection Guide, Scorpio L.R.S. Instrumentation. due to Scorpio Femoral Resection Guides have the potential to remove more bone than necessary.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Scorpio Femoral Resection Guides have the potential to remove more bone than necessary.
Recommended Action
Per FDA guidance
Product recall letters and product accountability forms were sent via FedEx to all Branches/sales agents on July 17, 2003. For the Canadian and International customers, the recall notification was also sent on July 17, 2003. All devices are to be returned to Howmedica Osteonics, Mahwah, NJ.
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
IN
Page updated: Jan 10, 2026