Stryker Howmedica Osteonics Corp. CuttingEdge Total Hip Instrumentation Surgical Protocol; Acetabular and Femoral Surgical Technique for Primary Press Fit and Cemented Hip Implants. Stryker Howmedica Osteonics. Surgical protocols instruct surgeons on proper surgical technique. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CuttingEdge Total Hip Instrumentation Surgical Protocol; Acetabular and Femoral Surgical Technique for Primary Press Fit and Cemented Hip Implants. Stryker Howmedica Osteonics. Surgical protocols instruct surgeons on proper surgical technique.
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Catalog Number/Code Number: LSP42.
Products Sold
Catalog Number/Code Number: LSP42.
Stryker Howmedica Osteonics Corp. is recalling CuttingEdge Total Hip Instrumentation Surgical Protocol; Acetabular and Femoral Surgical Technique f due to Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.
Recommended Action
Per FDA guidance
"Urgent Product Correction - Surgical Protocol" letters and Product Accountability Forms were sent to consignees via Fed Ex on August 31, 2009 and September 1, 2009 with return receipt. Notification letters described the issue, protocols affected, potential hazard and harm and risk mitigation. Direct questions about the recall by calling 1-201-972-2100 or Customer Service 1 -866-OR-ASSIST (1 -866-672-7747).
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