Secur-FitRecalls & reported problems across all models
Howmedica Osteonics Corp. · 45 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 138
- Deaths reported
- 1
- Injuries reported
- 133
- Recalls
- 0
We found 45 models of Secur-Fit by Howmedica Osteonics Corp. in the FDA's device registry (GUDID). Together they are named in 138 adverse event reports in the FDA's MAUDE database, received between Jan 12, 2017 and Oct 20, 2025 — classified as 1 death, 133 injuries, 4 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (57 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Secur-Fit problems
Device problems
- Insufficient Device Problem Information57
- Adverse Event Without Identified Device or Use Problem25
- Migration11
- Loss of Osseointegration10
- Degraded8
- Migration or Expulsion of Device8
- Malposition of Device6
- Osseointegration Problem6
Patient problems
- Injury78
- Bone Fracture(s)54
- Pain28
- Fall16
- Inadequate Osseointegration13
- Inflammation10
- Joint Dislocation9
- Reaction9
Secur-Fit models
45 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Secur-Fit 6052-0830SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate13 reports
- Secur-Fit 1601-08127Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous13 reports
- Secur-Fit 6052-0935SProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented11 reports
- Secur-Fit 6051-0935SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate6 reports
- Secur-Fit 6052-0730SProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented6 reports
- Secur-Fit 2051-2046Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate5 reports
- Secur-Fit 6051-0730SProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented5 reports
- Secur-Fit 6051-1035SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate5 reports
- Secur-Fit 6052-1035SProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented5 reports
- Secur-Fit 1601-07127Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented5 reports
- Secur-Fit 1601-09127Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous5 reports
- Secur-Fit 1601-09132Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous5 reports
- Secur-Fit 1601-10127Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous5 reports
- Secur-Fit 1601-08132Prosthesis, hip, semi-constrained, metal/polymer, uncemented4 reports
- Secur-Fit 6054-0913SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate3 reports
- Secur-Fit 6052-0625SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 death3 reports
- Secur-Fit 1601-07132Prosthesis, hip, semi-constrained, metal/polymer, uncemented3 reports
- Secur-Fit J6051-0625PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Secur-Fit 2051-2048Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate2 reports
- Secur-Fit 6054-0812SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate2 reports
- Secur-Fit 6051-0830SProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- Secur-Fit 6051-1140SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate2 reports
- Secur-Fit 1601-05132Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- Secur-Fit 1601-06127Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate2 reports
- Secur-Fit J6052-0830Prosthesis, hip, semi-constrained, metal/polymer, uncemented2 reports
- Secur-Fit J6051-0425Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 report
- Secur-Fit J6054-0711Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish1 report
- Secur-Fit J6054-1014Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 report
- Secur-Fit 2050-2044PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Secur-Fit 2051-2058Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Secur-Fit S-2337-HF06Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Secur-Fit 6054-0713SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Secur-Fit 6054-0711SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Secur-Fit 6054-0814SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Secur-Fit 6054-1014SProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Secur-Fit 6054-0915SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Secur-Fit 6054-1115SProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Secur-Fit 6052-1140SProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Secur-Fit 1601-06132Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- Secur-Fit 1601-10132Prosthesis, hip, hemi-, femoral, metal1 report
- Secur-Fit 1601-11127PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Secur-Fit 2051-2050PProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Secur-Fit J6051-0730Prosthesis, hip, hemi-, femoral, metal1 report
- Secur-Fit J6051-0830Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish1 report
- Secur-Fit J6052-0730Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 report
Recent Secur-Fit adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryOct 20, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT'S LEFT HEMI HIP WAS REVISED DUE TO A GREATER TROCHANTERIC FRACTURE. THE HEMI HIP WAS REMOVED, AND A NEW HEMI HIP INCLUDING A RESTORATION MODULAR STEM CONSTRUCT WAS IMPLANTED. REP CONFIRMED THERE WERE NO ALLEGATIONS AGAINST THE REVISED FEMORAL AND BIPOLAR HEADS, AND THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.
Patient problems: Bone Fracture(s)
MAUDE report 23334635 ↗InjuryOct 8, 2025Loss of Osseointegration; Osseointegration Problem; Loss of Osseointegration; Osseointegration Problem
IT WAS REPORTED THAT THE PATIENT'S HIP WAS REVISED DUE TO SHELL LOOSENING. THE SHELL, LINER AND HEAD WERE REVISED TO A COMPETITOR SHELL AND LINER WITH A NEW STRYKER HEAD. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASE BY THE HOSPITAL OR SURGEON.
Patient problems: Inadequate Osseointegration
MAUDE report 23248708 ↗InjuryJul 24, 2025Loss of Osseointegration; Loss of Osseointegration
PT. REPORTED; HAD RIGHT HIP IMPLANT IN (B(6) 2022 AND HAD MANY PROBLEMS WITH THE IMPLANT. PT. MENTIONED LOOSENING, IMMOBILITY, BURSITIS AND WEAR. IMPENDING REVISION TO REPLACE JOINT AND THE LINER DUE TO WEAR.
Patient problems: Ambulation or Postural Difficulties; Bursitis; Inadequate Osseointegration
MAUDE report 22599722 ↗InjuryMar 13, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO PAIN. THE STEM AND HEAD WERE REVISED. REP CONFIRMED THAT THERE WERE NO ADDITIONAL INTRA-OPERATIVE FINDINGS, AND THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.
Patient problems: Pain
MAUDE report 21593565 ↗InjuryFeb 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryDec 10, 2024Unintended Movement; Migration; Unintended Movement; Migration
SUBJECT SUSTAINED A FEMORAL FRACTURE AS A RESULT OF A FALL ON (B)(6)2022. ORIF WAS COMPLETED ON (B)(6)2022; SEE ATTACHED OPERATIVE NOTES AND ATTACHED CLINIC NOTES. SOME CONCERN OF FEMORAL SUBSIDENCE; FRACTURE HEALED AS OF (B)(6)2024. (NOTE THAT THE OPERATIVE NOTE HAS A DATE OF ORIGINAL SURGERY AS 2017 WHICH IS INCORRECT. SEE SUBSEQUENT FOLLOW-UP CLINIC NOTES CONFIRMING ORIGINAL SURGERY AS 2014.). SUBJECT WAS ENROLLED IN THE SECUR-FIT ADVANCE OUTCOMES STUDY 75.
Patient problems: Bone Fracture(s); Fall; Hip Fracture; Pain
MAUDE report 20897203 ↗InjuryOct 28, 2024Device Dislodged or Dislocated; Adverse Event Without Identified Device or Use Problem; Device Dislodged or Dislocated; Adverse Event Without Identified Device or Use Problem
PRIMARY THA SURGERY WAS PERFORMED ON (B)(6) 1997. REVISION SURGERY WAS PERFORMED FOR OSTEOLYSIS ON (B)(6) 2002. HEAD AND LINER WAS REPLACED. 2ND REVISION SURGERY WAS PERFORMED FOR DISLOCATION OF A JOINT ON (B)(6) 2016. CUP, LINER, HEAD, AND SCREW WERE REPLACED. 3RD REVISION SURGERY WAS PERFORMED FOR PSEUDOTUMOR CAUSED BY ARMD (B)(6) 2024. STEM, HEAD, LINER AND SCREWS WERE REPLACED. THIS PI IS FOR 2ND REVISION SURGERY.
Patient problems: Ambulation or Postural Difficulties; Joint Dislocation
MAUDE report 20552966 ↗InjurySep 26, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED DUE TO A FEMORAL PERIPROSTHETIC FRACTURE. A SECUR-FIT STEM AND CERAMIC HEAD WERE REVISED TO A RESTORATION MODULAR STEM, A NEW FEMORAL HEAD, AND DALL/MILES CABLES. REP CONFIRMED THAT THERE WERE NO ALLEGATIONS AGAINST THE REVISED FEMORAL HEAD, AND THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.
Patient problems: Bone Fracture(s)
MAUDE report 20309748 ↗InjuryMay 18, 2024Material Erosion; Patient Device Interaction Problem; Material Erosion; Patient Device Interaction Problem
POST THA SURGERY, THERE WAS A FINDING OF BONE ATROPHY IN THE ANTERIOR OF THE ACETABULUM, AND ARMD WAS SUSPECTED.
Patient problems: Cyst(s); Metal Related Pathology
MAUDE report 19348342 ↗InjuryApr 30, 2024Corroded; Corroded
IT WAS REPORTED BY CLAIMANT'S COUNSEL THAT THE PATIENT UNDERWENT LEFT THA ON (B)(6) 2014, AND WAS IMPLANTED WITH AN LFIT V40 FEMORAL HEAD AND A SECUR FIT ADVANCED STEM. RECENTLY HE FELT SOMETHING MOVING AND PRESENTED WITH LEFT HIP DISCOMFORT. HE WAS REVISED ON (B)(6) 2023, AND INTRAOPERATIVELY THE SURGEON NOTED "TRUNNION WAS VISUALIZED AND WAS CORRODED AND DEFORMED".
Patient problems: Discomfort
MAUDE report 19215331 ↗InjuryDec 22, 2023Loss of Osseointegration; Migration; Loss of Osseointegration; Migration
PATIENT UNDERWENT LEFT TOTAL HIP ARTHROPLASTY ON (B)(6) 2014 SUBSEQUENTLY HE DEVELOPED SEVERE THIGH PAIN, PAIN ON WEIGHTBEARING AND PAIN AT NIGHT. X-RAYS ALLEGEDLY DEMONSTRATED SETTLING OF HIS PROSTHESIS. HE WAS REVISED ON MAY 8, 2015 DUE TO ALLEGED LOOSENING OF HIS LEFT FEMORAL HIP COMPONENT.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 18382235 ↗InjuryNov 2, 2023Degraded; Degraded
IT IS REPORTED BY COUNSEL THAT CLAIMANT UNDERWENT LEFT THA ON (B)(6) 2015, AND WAS IMPLANTED WITH A SECUR-FIT ADVANCED HIP STEM AND A LFIT ANATOMIC V40 FEMORAL HEAD. HE WAS REVISED ON (B)(6) 2021 ALLEGEDLY DUE TO PAIN, ELEVATED METAL ION LEVELS, AND METALLOSIS AT THE HEAD-TRUNNION INTERFACE.
Patient problems: Foreign Body Reaction; Metal Related Pathology; Pain
MAUDE report 18054163 ↗InjuryJul 10, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
POSTOPERATIVELY, A LOOSENING DUE TO A PERIPROSTHETIC FEMUR FRACTURE WAS OCCURRED AND A REVISION SURGERY WAS PERFORMED.
Patient problems: Bone Fracture(s)
MAUDE report 17288509 ↗InjuryJun 16, 2023Osseointegration Problem; Osseointegration Problem
IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED DUE TO PAIN AND SUSPECTED STEM LOOSENING (LOOSENING WAS NEITHER CONFIRMED NOR DENIED BY THE SURGEON INTRA-OPERATIVELY). A STEM, HEAD, AND LINER WERE REVISED TO A RESTORATION MODULAR STEM CONSTRUCT, FEMORAL HEAD, ADM/ MDM POLY INSERT, AND MDM METAL LINER.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 17141499 ↗InjuryMay 18, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
DISLOCATED TOTAL LEFT HIP. SURGEON REPLACED FEMORAL STEM, FEMORAL HEAD AND MDM POLY INSERT. THE POLY HEAD CAME OUT OF THE METAL CUP LINER. SURGEON CHOSE TO REMOVE AND REPLACE STEM TO GIVE HIM THE ABILITY TO SHORTEN THE OVERALL STEM/NECK/ HEAD LENGTH.
Patient problems: Joint Dislocation
MAUDE report 16951315 ↗
Other Howmedica Osteonics Corp. products
- Triathlon608 models · 3,524 reports · 15 recalls
- Scorpio107 models · 113 reports · 28 recalls
- Trident160 models · 1,280 reports · 2 recalls
- Accolade57 models · 1,228 reports
- Duracon58 models · 65 reports · 16 recalls
- LFIT23 models · 852 reports
- TRIDENT II42 models · 188 reports · 12 recalls
- INSTRUMENT131 models · 290 reports · 7 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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