OMNI Mod HipRecalls & reported problems across all models
Omni Life Science, Inc. · 18 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 29
- Deaths reported
- 0
- Injuries reported
- 29
- Recalls
- 0
We found 18 models of OMNI Mod Hip by Omni Life Science, Inc. in the FDA's device registry (GUDID). Together they are named in 29 adverse event reports in the FDA's MAUDE database, received between Mar 31, 2017 and May 8, 2025 — classified as 29 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (6 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 OMNI Mod Hip problems
Device problems
- Adverse Event Without Identified Device or Use Problem7
- Appropriate Device Problem Term/Code Not Available7
- Insufficient Device Problem Information6
- Break3
- Device Dislodged or Dislocated3
- Unstable2
- Device Operates Differently Than Expected1
- Fracture1
Patient problems
- No Code Available6
- Joint Dislocation5
- Unspecified Infection4
- Bone Fracture(s)3
- Failure of Implant3
- Fall2
- Insufficient Information2
- Pain2
OMNI Mod Hip models
18 models, most reported first. Each model has its own page with its reports, recalls and device details.
- OMNI Mod Hip 151456Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- OMNI Mod Hip 151306Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate3 reports
- OMNI Mod Hip 151003Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- OMNI Mod Hip 230205PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- OMNI Mod Hip 230210PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- OMNI Mod Hip 230310PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- OMNI Mod Hip 230400PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- OMNI Mod Hip 230410PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- OMNI Mod Hip 150902PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- OMNI Mod Hip 151153Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- OMNI Mod Hip 151154PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- OMNI Mod Hip 151305Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- OMNI Mod Hip 151455Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- OMNI Mod Hip 151606PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- OMNI Mod Hip 230405PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- OMNI Mod Hip 230610PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- OMNI Mod Hip 231210PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- OMNI Mod Hip 231310PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
Recent OMNI Mod Hip adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryMay 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2025. THE ORIGINAL SURGERY IS DATED (B)(6) 2010. THE REASON FOR REVISION IS REPORTED DISLOCATION. DURING THE SURGERY, THE ORIGINAL FEMORAL NECK AND HEAD WERE REMOVED AND REPLACED WITH NEW IMPLANTS.
Patient problems: Joint Dislocation
MAUDE report 21984348 ↗InjuryFeb 14, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2023. THE ORIGINAL SURGERY DATE IS ON (B)(6) 2023. THE REASON FOR REVISION IS REPORTED PATIENT FALL THAT RESULTED IN PERI-PROSTHETIC FRACTURE DURING THE REVISION STEM AND MODULAR NECK WERE REMOVED AND REPLACED WITH NEW DEVICES.
Patient problems: Fall
MAUDE report 16375655 ↗InjuryAug 25, 2022Insufficient Device Problem Information; Insufficient Device Problem Information
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP SURGERY ON (B)(6) 2022. THE ORIGINAL SURGERY OCCURRED IN (B)(6) 2022. THE SURGERY OCCURRED BECAUSE OF REPORTED INFECTION DURING THE REVISION STEM AND MODULAR NECK AND HEAD WERE REMOVED AND REPLACED WITH NEW DEVICES.
Patient problems: Unspecified Infection
MAUDE report 15298789 ↗InjuryAug 9, 2022Break
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2022. THE ORIGINAL SURGERY DATE IS (B)(6) 2022. THE REASON FOR REVISION IS REPORTED FEMORAL FRACTURE DURING THE REVISION, THE STEM, MODULAR NECK AND FEMORAL HEAD WERE REMOVED AND REPLACED WITH NON OMNI DEVICES.
Patient problems: Failure of Implant
MAUDE report 15192619 ↗InjuryApr 4, 2022Adverse Event Without Identified Device or Use Problem
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2022. THE ORIGINAL SURGERY DATE IS (B)(6) 2022. THE REASON FOR REVISION IS REPORTED PATIENT FALL THAT RESULTED IN PERI-PROSTHETIC FRACTURE DURING THE REVISION STEM AND MODULAR NECK WERE REMOVED AND REPLACED WITH NON-OMNI DEVICES.
Patient problems: Bone Fracture(s); Fall
MAUDE report 13997665 ↗InjuryMar 24, 2022Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2022. THE ORIGINAL SURGERY DATE WAS (B)(6) 2022. THE REASON FOR REVISION REPORTED IS SUBSIDED STEM. DURING THE REVISION A STEM, MODULAR NECK AND FEMORAL HEAD WAS REMOVED AND REPLACED WITH NEW COMPONENTS.
Patient problems: Insufficient Information
MAUDE report 13873778 ↗InjurySep 9, 2021Adverse Event Without Identified Device or Use Problem
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2021. THE ORIGINAL SURGERY OCCURRED ON (B)(6) 2021. THE REVISION SURGERY OCCURRED BECAUSE OF POSSIBLE INFECTION. DURING THE REVISION ALL OF THE IMPLANTS WERE REMOVED AND REPLACED BY NEW COMPONENTS.
Patient problems: Unspecified Infection
MAUDE report 12449120 ↗InjuryMay 28, 2021Appropriate Device Problem Term/Code Not Available
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2021. THE ORIGINAL SURGERY OCCURRED ON (B)(6) 2014. THE REASON FOR REVISION IS REPORTED PATIENT PAIN. DURING THE REVISION, THE ORIGINAL STEM AND MODULAR NECK WERE REMOVED. THE STEM WAS REPLACED WITH A NON-OMNI COMPONENT.
Patient problems: Pain
MAUDE report 11903096 ↗InjuryFeb 3, 2021Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2021. THE ORIGINAL SURGERY IS DATED (B)(6) 2010. THE REASON FOR REVISION IS REPORTED DISLOCATION. DURING THE SURGERY, ORIGINAL FEMORAL HEAD AND MODULAR NECK WERE REPLACED FOR NEW COMPONENTS.
Patient problems: Joint Dislocation
MAUDE report 11277063 ↗InjuryOct 16, 2020Break; Break
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2020. THE ORIGINAL SURGERY IS DATED (B)(6) 2004. THE REASON FOR REVISION IS ANTI-ROTATION PIN BREAKAGE. DURING THE REVISION, THE ORIGINAL FEMORAL HEAD, MODULAR NECK AND MODULAR STEM WERE REMOVED AND REPLACED WITH NEW COMPONENTS.
Patient problems: Insufficient Information
MAUDE report 10693660 ↗InjuryJan 10, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2019. THE ORIGINAL SURGERY IS DATED (B)(6) 2018. THE REASON FOR REVISION IS REPORTED DISLOCATION. DURING THE SURGERY, THE ORIGINAL FEMORAL HEAD AND MODULAR NECK WERE REMOVED AND REPLACED FOR NEW COMPONENTS.
Patient problems: Joint Dislocation
MAUDE report 9578325 ↗InjuryJan 10, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2019. THE ORIGINAL SURGERY IS DATED (B)(6) 2012. THE REASON FOR REVISION IS REPORTED DISLOCATION. DURING THE REVISION, THE ORIGINAL MODULAR NECK WAS REMOVED AND REPLACED WITH A NEW COMPONENT.
Patient problems: Joint Dislocation
MAUDE report 9578232 ↗InjuryNov 21, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2019. THE ORIGINAL SURGERY IS DATED (B)(6) 2015. THE REASON FOR REVISION IS REPORTED PATIENT PAIN. DURING THE REVISION, THE MODULAR NECK AND STEM WERE REMOVED AND REPLACED WITH NON-OMNI PRODUCT.
Patient problems: Pain
MAUDE report 9356544 ↗InjuryAug 6, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
A COMPLAINT WAS INITIATED FOR A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2019. THE ORIGINAL SURGERY IS DATED (B)(6) 2010. THE REASON FOR REVISION IS REPORTED HIGH METEL ION LEVELS. DURING THE REVISION, THE ORIGINAL OMNI NECK, NON-OMNI LINER AND NON-OMNI HEAD WERE REMOVED AND REPLACED WITH NEW COMPONENTS.
Patient problems: Toxicity
MAUDE report 8865818 ↗InjuryDec 11, 2018Appropriate Device Problem Term/Code Not Available
THE COMPLAINT INVOLVED A PATIENT WHO UNDERWENT A HIP REVISION SURGERY ON (B)(6) 2018. THE ORIGINAL SURGERY IS DATED (B)(6) 2004. THE REVISION SURGERY OCCURRED BECAUSE OF A REPORTED PSEUDOTUMOR. DURING THE REVISION, THE ORIGINAL OMNI MODULAR NECK AND FEMORAL HEAD WERE REMOVED AND REPLACED WITH NEW COMPONENTS.
Patient problems: No Code Available
MAUDE report 8150180 ↗
Other Omni Life Science, Inc. products
All Omni Life Science, Inc. devices →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.
How reports and recalls are matched · Editorial policy · Report an error on this page