RecallDepth

Triathlon Total Stabilizer Femoral Component; For Use with TS Components; Sterile, Made in the USA Stryker Orthopaedics, Mahwah, NJ 07430. The Triathlon Total Knee System components are intended for use in primary and revision total knee arthroplasty to alleviate pain and restore function.

Company
Stryker Howmedica Osteonics Corp.
Recall Initiated
December 10, 2009
Posted
February 1, 2010
Terminated
August 28, 2012
Recall Number
Z-0760-2010
Quantity
10
Firm Location
Mahwah, NJ

Reason for Recall

Triathlon TS femoral components may have been damaged during manufacturing, possibly preventing the assembly of a stem extension.

Distribution

Worldwide Distribution -- United States (DE, NC, OH. MI, TX, CA, MA, NJ, TN, KS, GA, FL, AL, IN, MN, MD, NE, AR, OK, CO, AZ, OR, and MA), Australia, United Kingdom and Canada.

Lot / Code Info

Catalog number: 5512-F-501; Lot codes: XAVN, XAVP and XBAL.

Root Cause

Nonconforming Material/Component

Action Taken

An "Urgent Product Recall" Letter dated December 10, 2009 was sent by Federal Express to all Stryker Branches, Chief of Orthopaedics, Hospital Risk Management and Surgeons. The letter described the affected product, issue and potential hazards. Consignees were instructed to complete Product Recall Acknowledgement Form and return to Stryker Orthopaedics via fax at 1-201-831-6069. All questions regarding the recall should be directed to Stryker Orthopaedics at 1-201-972-2100.

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