Stryker Howmedica Osteonics Corp. OmniFit Eon 127 degree and 132 degree Surgical Protocol; Stryker. Surgical protocols instruct surgeons on proper surgical technique. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OmniFit Eon 127 degree and 132 degree Surgical Protocol; Stryker. Surgical protocols instruct surgeons on proper surgical technique.
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Catalog Number/Lot Code: LSP48.
Products Sold
Catalog Number/Lot Code: LSP48.
Stryker Howmedica Osteonics Corp. is recalling OmniFit Eon 127 degree and 132 degree Surgical Protocol; Stryker. Surgical protocols instruct surge 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