Stryker Howmedica Osteonics Corp. Navigation Reamer T-handle; Non Sterile; Howmedica Osteonics, 325 Corporate Drive, Mahwah, NJ 07430. Intended for use in orthopaedic surgery to interface with various cutting instruments and drivers. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Navigation Reamer T-handle; Non Sterile; Howmedica Osteonics, 325 Corporate Drive, Mahwah, NJ 07430. Intended for use in orthopaedic surgery to interface with various cutting instruments and drivers.
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Catalog Number: 2124-2100, Lot Codes: ALZH05 and ALZE32.
Products Sold
Catalog Number: 2124-2100; Lot Codes: ALZH05 and ALZE32.
Stryker Howmedica Osteonics Corp. is recalling Navigation Reamer T-handle; Non Sterile; Howmedica Osteonics, 325 Corporate Drive, Mahwah, NJ 07430. due to Stryker Orthopaedics learned that the T-handles have the potential to not engage and not attach to the reamer properly.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Stryker Orthopaedics learned that the T-handles have the potential to not engage and not attach to the reamer properly.
Recommended Action
Per FDA guidance
Stryker Orthopaedics issued notification dated August 8, 2005 via Federal Express. Consignees were informed of the affected product and necessary steps to take for product replacement. For further information, contact Stryker at (201) 831-5825.
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