Stryker Instruments Div. of Stryker Corporation Stryker Navigation Pin for use with the Stryker Navigation System, 3 mm x 100 mm, Stryker, Kalamazoo, MI; Part 6007-003-100. Stryker Navigation Pin for use with the Stryker navigation system is used for trauma and orthopedic applications, e.g. hip and knee modules. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker Navigation Pin for use with the Stryker Navigation System, 3 mm x 100 mm, Stryker, Kalamazoo, MI; Part 6007-003-100. Stryker Navigation Pin for use with the Stryker navigation system is used for trauma and orthopedic applications, e.g. hip and knee modules.
Brand
Stryker Instruments Div. of Stryker Corporation
Lot Codes / Batch Numbers
All units distributed prior to 6/5/08.
Products Sold
All units distributed prior to 6/5/08.
Stryker Instruments Div. of Stryker Corporation is recalling Stryker Navigation Pin for use with the Stryker Navigation System, 3 mm x 100 mm, Stryker, Kalamazoo due to Instructions have been updated to include new warnings regarding percutaneous pin placement during surgery in order to mitigate the risk of femur frac. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Instructions have been updated to include new warnings regarding percutaneous pin placement during surgery in order to mitigate the risk of femur fractures.
Recommended Action
Per FDA guidance
Consignees were notified via letter dated 6/5/08 providing them with additional warnings and instructions for use for these products. Contact Stryker Customer Service at 1-800-800-4236, ext. 3808.
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