Z-0893-2009

Secur-Fit Max Hip Stem These devices are modular components of a total hip system. These femoral stems are...

Name: Z-0893-2009 Secur-Fit Max Hip Stem These devices are modular components of a total hip system. These femoral 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 Secur-Fit Max Hip Stem These devices are modular components of a total hip system. These femoral stems are intended for use with femoral heads and acetabular... 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-0893-2009
Status: Terminated
Initiated: 2008-11-13
Posted: 2009-01-26
Terminated: 2010-01-20
Recalling firm: Howmedica Osteonics Corp
Product: Secur-Fit Max Hip Stem These devices are modular components of a total hip system. These femoral stems are intended for use with femoral heads and acetabular components in primary or revision total hip arthroplasty.
Product code: LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
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: 6051-0625S SECUR-FIT MAX 132 HIP STEM #6 HKNMME, 6051-0730S SECUR-FIT MAX 132 HIP STEM #7 K03MME, 6051-0730S SECUR-FIT MAX 132 HIP STEM #7 K08MME, 6051-0830S SECUR-FIT MAX 132 HIP STEM #8 E56MLE, 6051-0830S SECUR-FIT MAX 132 HIP STEM #8 J41MLE, 6051-0935S SECUR-FIT MAX 132 HIP STEM #9 EN1MME, 6051-1035S SECUR-FIT MAX 132 HIP STEM #10 70PMME, 6051-1140S SECUR-FIT MAX 132 HIP STEM #11 4PMMME, 6051-1140S SECUR-FIT MAX 132 HIP STEM #11 901MME, 6052-0830S SECUR-FIT MAX 127 HIP STEM #8 V3PMLE, 6052-0935S SECUR-FIT MAX 127 HIP STEM #9 5ERMME, 6052-1035S SECUR-FIT MAX 127 HIP STEM #10 69WMME, 6052-1035S SECUR-FIT MAX 127 HIP STEM #10 AL8MME and 6052-1240S SECUR-FIT MAX 127 HIP STEM #12 EP4MME

Product code LZO

K041170Class IISecur-Fit Ha and Secur-Fit Plus Hip StemsHowmedica Osteonics Corp. / cleared 2004-11-09

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)