Stryker Howmedica Osteonics Corp. Stryker Orthopaedics Bone Screw; Dia 6.5 mm; Lnth: 25 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker Orthopaedics Bone Screw; Dia 6.5 mm; Lnth: 25 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures.
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Catalog number: 2020-6525-1, Lot number HRJMME, Exp. 8/20/2013.
Products Sold
Catalog number: 2020-6525-1; Lot number HRJMME, Exp. 8/20/2013.
Stryker Howmedica Osteonics Corp. is recalling Stryker Orthopaedics Bone Screw; Dia 6.5 mm; Lnth: 25 mm; Sterile: Made in the USA; Stryker Osteonic due to Raw material supplied by a third party used to manufacture various medical devices does not comply with metallurgical requirements outlines in ASTM st. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Raw material supplied by a third party used to manufacture various medical devices does not comply with metallurgical requirements outlines in ASTM standard for titanium surgical implants.
Recommended Action
Per FDA guidance
Stryker Orthopaedics issued "Urgent Product Recall" letters via Federal Express priority overnight beginning June 26, 2009 to Branches, Hospital Risk Management and Chief of Orthopaedics and Surgeons. All users are requested to examine their inventory, retrieve all affected product and return for reconciliation to Stryker Orthopaedics. Users are also requested to complete the enclosed Product Accountability Form and fax with necessary information to the firm at 1-201-831-6069. For further information, contact Stryker Orthopaedics at 1-201-831-5970.
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