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FDA Medical Device Recalls (openFDA)

Stryker Howmedica Osteonics Corp.: Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 45 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 number
Z-2122-2009
Recalling firm
Stryker Howmedica Osteonics Corp.
Product
Stryker Orthopaedics Cancellous Bone Screw; Dia 6.5 mm; Lnth: 45 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.
Status
Terminated
Initiated
2009-06-26
Posted
2009-09-14
Terminated
2010-07-27
Reason
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
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
51,113 total - all sizes.
Distribution
Worldwide Distribution
Lot, serial or model codes
Catalog number: 2030-6545-1; 6.5 CANCELLOUS BONE SCREW 45mm EA9MKE 18-Jun-2013 6.5 CANCELLOUS BONE SCREW 45mm KKXMKE 22-Jun-2013 6.5 CANCELLOUS BONE SCREW 45mm NN8MKE 24-Jun-2013 6.5 CANCELLOUS BONE SCREW 45mm 164MLE 06-Jul-2013 6.5 CANCELLOUS BONE SCREW 45mm 8J8MLE 14-Jul-2013 6.5 CANCELLOUS BONE SCREW 45mm 8J9MLE 14-Jul-2013 6.5 CANCELLOUS BONE SCREW 45mm 8JAMLE 14-Jul-2013 6.5 CANCELLOUS BONE SCREW 45mm KKTMLE 22-Jul-2013 6.5 CANCELLOUS BONE SCREW 45mm KKWMLE 23-Jul-2013 6.5 CANCELLOUS BONE SCREW 45mm KTEMLE 25-Jul-2013 6.5 CANCELLOUS BONE SCREW 45mm 6N6MNE 16-Sep-2013 6.5 CANCELLOUS BONE SCREW 45mm 6N7MNE 16-Sep-2013 6.5 CANCELLOUS BONE SCREW 45mm 9TRMNE 21-Sep-2013 6.5 CANCELLOUS BONE SCREW 45mm MER98P 19-Nov-2013 6.5 CANCELLOUS BONE SCREW 45mm MER98R 19-Nov-2013 6.5 CANCELLOUS BONE SCREW 45mm MER9VE 20-Nov-2013 6.5 CANCELLOUS BONE SCREW 45mm MER9VK 20-Nov-2013 6.5 CANCELLOUS BONE SCREW 45mm MER9VM 20-Nov-2013 6.5 CANCELLOUS BONE SCREW 45mm MET278 07-Dec-2013 6.5 CANCELLOUS BONE SCREW 45mm MET3LW 11-Dec-2013 6.5 CANCELLOUS BONE SCREW 45mm MET3M1 11-Dec-2013 6.5 CANCELLOUS BONE SCREW 45mm MET8YD 18-Dec-2013 6.5 CANCELLOUS BONE SCREW 45mm MET8YE 30-Dec-2013 6.5 CANCELLOUS BONE SCREW 45mm METH2A 06-Jan-2014 6.5 CANCELLOUS BONE SCREW 45mm METH2D 06-Jan-2014 6.5 CANCELLOUS BONE SCREW 45mm METNRR 07-Jan-2014 6.5 CANCELLOUS BONE SCREW 45mm METNRT 07-Jan-2014 6.5 CANCELLOUS BONE SCREW 45mm MHA25W 11-Jan-2014 6.5 CANCELLOUS BONE SCREW 45mm MHA25X 11-Jan-2014 6.5 CANCELLOUS BONE SCREW 45mm MHA25Y 11-Jan-2014 6.5 CANCELLOUS BONE SCREW 45mm MET279 14-Jan-2014
510(k) numbers
["K873251"]
PMA numbers
not on file
Product code
HWC
Firm FEI
3003070421
Firm city
Mahwah
Firm state
NJ
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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