Secur-Fit 1601-07132Recalls & reported problems
Howmedica Osteonics Corp. · 132 Degree Neck Angle V40 Hip Stem · Class 2 · Implant
All models of Secur-Fit (45)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327021301), received between Apr 22, 2017 and Dec 12, 2018 — classified as 3 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information2
- Migration1
Patient problems
- Bone Fracture(s)3
- Injury3
- Fall1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryDec 12, 2018Migration; Migration
IT WAS REPORTED THAT PATIENT'S LEFT HIP WAS REVISED DUE A PERIPROSTHETIC FEMORAL FRACTURE AND STEM SUBSIDENCE AFTER PATIENT FELL. THE SECURFIT ADVANCED STEM, BIOLOX 32 +0 HEAD, AND 32MM 0° C LINER WERE REVISED TO A COMPETITOR MODULAR STEM CONSTRUCT AND FEMORAL HEAD WITH A STRYKER ADM/MDM LINER CONSTRUCT AND 4 CABLE AND SLEEVE SETS.
Patient problems: Bone Fracture(s); Fall; Injury
MAUDE report 8157894 ↗InjurySep 14, 2017Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT THE SURGEON PERFORMED A REVISION ON THE PATIENT'S LEFT HIP DUE TO A FEMORAL FRACTURE SUSTAINED WHILE WORKING WITH CATTLE. PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO DELAYS.
Patient problems: Bone Fracture(s); Injury
MAUDE report 6865710 ↗InjuryApr 22, 2017Insufficient Device Problem Information; Insufficient Device Problem Information
SALES REP REPORTED PATIENT SUFFERED A PERIPROSTHETIC FRACTURE 1 MONTH POST OPERATIVE.
Patient problems: Bone Fracture(s); Injury
MAUDE report 6513738 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, uncemented devices
- LFIT 6260-9-136Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented166 reports
- Trident 623-00-36EHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented112 reports
- Accolade 6021-0435Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented88 reports
- EXETER 0580-1-044Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 recall22 reports
- Endo-Model SL Knee Prosthesis System 16-2840/02WALDEMAR LINK GmbH & Co. KG · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented1 recall17 reports
- Endo-Model SL Knee Prosthesis System 16-2840/05WALDEMAR LINK GmbH & Co. KG · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented1 recall12 reports
- Trident 623-10-36EHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented57 reports
- LFIT 6260-9-336Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented56 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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