Z-0890-2009

Triathlon-Press-Fit Stem These devices are modular components of a total knee system. These modular stems are...

Name: Z-0890-2009 Triathlon-Press-Fit Stem These devices are modular components of a total knee system. These modular stems are...
Creator: Stryker Howmedica Osteonics Corp.
Published: 2008-11-13
License: https://open.fda.gov/license/

Howmedica Osteonics Corp / initiated 2008-11-13 / Terminated / root cause: packaging

FDA source

Stryker Howmedica Osteonics Corp. began a recall of Triathlon-Press-Fit Stem These devices are modular components of a total knee system. These modular stems are intended for use with femoral and tibial... on 2008-11-13. The reason FDA records is "Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0890-2009
Status: Terminated
Initiated: 2008-11-13
Posted: 2009-01-26
Terminated: 2010-01-20
Recalling firm: Howmedica Osteonics Corp
Product: Triathlon-Press-Fit Stem These devices are modular components of a total knee system. These modular stems are intended for use with femoral and tibial components in primary or revision total knee arthroplasty.
Product code: JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Reason for recall: Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices.
Root cause tag: packaging
FDA root cause: Packaging
Action: Recall notification letters were sent via Federal Express on November 21, 2008 to Stryker Branches/Agencies, Hospital Risk Management, Chief of Orthopaedics and Surgeon. The letters explained the problem and indicated that there are no risk factors. Contact Stryker Orthopaedics for additional information at 1-201-831-5718.
Quantity in commerce: 322 total units - all types
Distribution: Nationwide. OUS: Australia, Canada, Japan, Argentina, Brazil, Germany, Spain, Columbia, Guatemala and Sweden.
Product codes and lots: 5565-S-015 TRI PRESS-FIT STEM 15MM X 100MM M3M07B, 5565-S-016 TRI PRESS-FIT STEM 16MM X 100MM M3M01B, 5565-S-016 TRI PRESS-FIT STEM 16MM X 100MM M3M01E, 5565-S-017 TRI PRESS-FIT STEM 17MM X 100MM M3M03A, 5566-S-012 TRI PRESS-FIT STEM 12X150MM M3L11F, 5566-S-013 TRI PRESS-FIT STEM 13X150MM M3L12B, and 5566-S-018 TRI PRESS-FIT STEM 18X150MM M3L17D

Product code JWH

K070095Class IITriathlon Ts Knee SystemHowmedica Osteonics Corp. / cleared 2007-06-01

MDM coverage of this record lists here, newest first.

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)