Secur-Fit Max Hip Stem recallZ-0893-2009 · Stryker Howmedica Osteonics Corp. · initiated Nov 13, 2008
Terminated All recalls posted in January 2009
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Stryker Howmedica Osteonics Corp. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices.
FDA root cause category: Packaging
What the company is doing
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.
Recall details
- Recall number
- Z-0893-2009
- Recall class
- Not yet classified by the FDA
- Status
- Terminated
- Initiated by the company
- Nov 13, 2008
- Posted by the FDA
- Jan 26, 2009
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Quantity
- 322 total units - all types
- Product code
- LZO
- FDA submissions
- K041170
- Distribution
- Nationwide. OUS: Australia, Canada, Japan, Argentina, Brazil, Germany, Spain, Columbia, Guatemala and Sweden.
Product description
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.
Code information (models, lots, serial numbers)
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
Other devices under the same FDA submission
19 devices cleared under K041170 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- Secur-Fit 6052-0830SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate13 reports
- Secur-Fit 6052-0935SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented11 reports
- Secur-Fit 6051-0935SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate6 reports
- Secur-Fit 6052-0730SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented6 reports
- Secur-Fit 6051-0730SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented5 reports
- Secur-Fit 6051-1035SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate5 reports
- Secur-Fit 6052-1035SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented5 reports
- Secur-Fit 6054-0913SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate3 reports
- Secur-Fit 6052-0625SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 death3 reports
- Secur-Fit 6054-0812SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate2 reports
- Secur-Fit 6051-0830SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- Secur-Fit 6051-1140SHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate2 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 50485).
- Z-0891-2009 · TerminatedOmnifit HA 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 …
- Z-0894-2009 · TerminatedPrimary Secur-fit Plus 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 componen…
- Z-0896-2009 · TerminatedOmnifit HFX 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…
- Z-0898-2009 · TerminatedOmnifit FC Cemented 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 prima…
- Z-0899-2009 · TerminatedOmnifit Eon 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 revisio…
- Z-0902-2009 · TerminatedSecur-Fit ARC/HA Collar 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 p…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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