Stryker Instruments, Instruments Div. Stryker Navigation System - Hip Module Patient Tracker, green; Model 6007-005-000. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker Navigation System - Hip Module Patient Tracker, green; Model 6007-005-000.
Brand
Stryker Instruments, Instruments Div.
Lot Codes / Batch Numbers
Serial numbers PG04-0001 through PG04-0017.
Products Sold
Serial numbers PG04-0001 through PG04-0017.
Stryker Instruments, Instruments Div. is recalling Stryker Navigation System - Hip Module Patient Tracker, green; Model 6007-005-000. due to The tracker is not locking adequately to the anchoring pin, resulting in unacceptable movement, which will affected the patient tracker system.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The tracker is not locking adequately to the anchoring pin, resulting in unacceptable movement, which will affected the patient tracker system.
Recommended Action
Per FDA guidance
Sales force was notified these pre-launch devices are not to be used for surgical use via e-mail and telephone calls on 7/14/04.
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