Z-2123-2009

Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 50 mm; Sterile: Made in the USA; Stryker...

Name: Z-2123-2009 Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 50 mm; Sterile: Made in the USA; Stryker...
Creator: Stryker Howmedica Osteonics Corp.
Published: 2009-06-26
License: https://open.fda.gov/license/

Howmedica Osteonics Corp / initiated 2009-06-26 / Terminated / root cause: manufacturing process

FDA source

Stryker Howmedica Osteonics Corp. began a recall of Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 50 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430... on 2009-06-26. The reason FDA records is "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". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-2123-2009
Status: Terminated
Initiated: 2009-06-26
Posted: 2009-09-14
Terminated: 2010-07-27
Recalling firm: Howmedica Osteonics Corp
Product: Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 50 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.
Product code: HWC Screw, Fixation, Bone
Reason for recall: 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.
Root cause tag: manufacturing process
FDA root cause: Nonconforming Material/Component
Action: 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.
Quantity in commerce: 51,113 total - all sizes.
Distribution: Worldwide Distribution
Product codes and lots: Catalog number: 2030-6550-1; 6.5 CANCELLOUS BONE SCREW 50mm KKMMKE 22-Jun-2013 6.5 CANCELLOUS BONE SCREW 50mm NMXMKE 25-Jun-2013 6.5 CANCELLOUS BONE SCREW 50mm R89MKE 27-Jun-2013 6.5 CANCELLOUS BONE SCREW 50mm 8K6MLE 14-Jul-2013 6.5 CANCELLOUS BONE SCREW 50mm 8K4MLE 14-Jul-2013 6.5 CANCELLOUS BONE SCREW 50mm MAJMLE 25-Jul-2013 6.5 CANCELLOUS BONE SCREW 50mm MAHMLE 28-Jul-2013 6.5 CANCELLOUS BONE SCREW 50mm HVWMME 22-Aug-2013 6.5 CANCELLOUS BONE SCREW 50mm 3J4MNE 09-Sep-2013 6.5 CANCELLOUS BONE SCREW 50mm 5V4MNE 11-Sep-2013 6.5 CANCELLOUS BONE SCREW 50mm MER715 18-Nov-2013 6.5 CANCELLOUS BONE SCREW 50mm MER714 18-Nov-2013 6.5 CANCELLOUS BONE SCREW 50mm MERDR9 23-Nov-2013 6.5 CANCELLOUS BONE SCREW 50mm MERDRA 23-Nov-2013 6.5 CANCELLOUS BONE SCREW 50mm MERP11 05-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm MET0XY 07-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm MET27A 10-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm MET3M4 10-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm MET3M6 12-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm MET8YH 21-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm METE5N 21-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm METDV8 21-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm METNRN 04-Jan-2014 6.5 CANCELLOUS BONE SCREW 50mm METNRP 04-Jan-2014 6.5 CANCELLOUS BONE SCREW 50mm MHA0L5 11-Jan-2014 6.5 CANCELLOUS BONE SCREW 50mm MHA0MP 11-Jan-2014

Product code HWC

K873251Class IIOmnifit Bone ScrewOsteonics Corp. / cleared 1987-09-18

China's FDA-registered implant bench is 151 establishments of 4,70415 SEP 2026 / by Medical Device Manufacturing

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)