Stryker Instruments Div. of Stryker Corporation Stryker VertePort , 11 G Cement Cannula, REF 306-510 , Qty 18; For use with the Stryker PCD Precision System and ACM Delivery System, Rx only, sterile, Stryker Instruments, Kalamazoo, MI. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker VertePort , 11 G Cement Cannula, REF 306-510 , Qty 18; For use with the Stryker PCD Precision System and ACM Delivery System, Rx only, sterile, Stryker Instruments, Kalamazoo, MI.
Brand
Stryker Instruments Div. of Stryker Corporation
Lot Codes / Batch Numbers
All Lots-BB43, BDL5, BE0M, BE1D, BE77, BF4K, BMWJ, BNW8, BNW9 and BQ5W
Products Sold
All Lots-BB43, BDL5, BE0M, BE1D, BE77, BF4K, BMWJ, BNW8, BNW9 and BQ5W
Stryker Instruments Div. of Stryker Corporation is recalling Stryker VertePort , 11 G Cement Cannula, REF 306-510 , Qty 18; For use with the Stryker PCD Precisi due to Mis-labeing; The instructions for use include a use for which the device is not intended. (Device not approved to capture a bone biopsy). Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Mis-labeing; The instructions for use include a use for which the device is not intended. (Device not approved to capture a bone biopsy)
Recommended Action
Per FDA guidance
Consignees were notified via Medical Device Recall Notification letter dated 2/13/08 to read the enclosed instructions for use, remove all old instructions for use at the consignee location and replace them with the new instructions for use, and to discard the old instructions for use.
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