TaperFit Cemented Hip SystemRecalls & reported problems across all models
Corin Ltd · 8 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 11
- Recalls
- 1
We found 8 models of TaperFit Cemented Hip System by Corin Ltd in the FDA's device registry (GUDID). Together they are named in 12 adverse event reports in the FDA's MAUDE database, received between Nov 6, 2024 and Jul 29, 2026 — classified as 11 injuries, 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (3 reports).
1 FDA recall record name at least one of these models by its device identifier.
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
TaperFit Cemented Hip System recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jul 12, 2022Terminated
Some of the devices did not pass fatigue testing.
Z-1667-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported TaperFit Cemented Hip System problems
Device problems
- Adverse Event Without Identified Device or Use Problem5
- Insufficient Device Problem Information3
- Fracture2
- Loosening of Implant Not Related to Bone-Ingrowth2
- Material Integrity Problem1
Patient problems
- Bone Fracture(s)3
- Pain2
- Fall1
- Joint Impingement1
- No Clinical Signs, Symptoms or Conditions1
- Periprosthetic fracture1
- Unequal Limb Length1
- Unspecified Infection1
TaperFit Cemented Hip System models
8 models, most reported first. Each model has its own page with its reports, recalls and device details.
- TaperFit Cemented Hip System 588.3800Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall2 reports
- TaperFit Cemented Hip System 588.4501Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- TaperFit Cemented Hip System 588.4503Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- TaperFit Cemented Hip System 588.4500Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- TaperFit Cemented Hip System 340.450Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- TaperFit Cemented Hip System 588.3600Prosthesis, hip, femoral component, cemented, metal1 report
- TaperFit Cemented Hip System 588.3803Prosthesis, hip, femoral component, cemented, metal1 report
- TaperFit Cemented Hip System 588.4502Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
Recent TaperFit Cemented Hip System adverse event reports
The 12 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJul 29, 2026Adverse Event Without Identified Device or Use Problem
TaperFit revision after approximately 10 years and 8 months due to a peri-prosthetic fracture of the left femur following a fall.
Patient problems: Bone Fracture(s)
MAUDE report 50066735 ↗InjuryJun 8, 2026Adverse Event Without Identified Device or Use Problem
TRINITY DUAL MOBILITY / TAPERFIT REVISION OF THE STEM, BIOLOX DELTA CERAMIC HEAD AND ECIMA INSERT AFTER APPROXIMATELY 6 YEARS AND 3 MONTHS DUE TO A PERI-PROSTHETIC FRACTURE FOLLOWING A FALL.
Patient problems: Periprosthetic fracture
MAUDE report 25426491 ↗MalfunctionJun 4, 2026Material Integrity Problem
IT WAS REPORTED BY THE CSSD AT MAITLAND PUBLIC HOSPITAL AUSTRALIA THAT 2 METAFIX STRAIGHT HANDLES WERE FOUND TO HAVE SHARP EDGES THAT CUT SOMEONE'S FINGER. MORE INFORMATION REGARDING THE REPORTED INJURY AND SERIOUSNESS OF THE CUT HAS BEEN REQUESTED BUT NO FURTHER INFORMATION RECEIVED.
Patient problems: Unspecified Tissue Injury
MAUDE report 25394716 ↗InjuryFeb 5, 2026Insufficient Device Problem Information
TAPERFIT / TRINITY REVISION OF THE STEM AND BIOLOX DELTA CERAMIC HEAD DUE TO A LEG LENGTH DISCREPANCY.
Patient problems: Unequal Limb Length
MAUDE report 24269318 ↗InjuryDec 22, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
TAPERFIT / TRINITY DUAL MOBILITY REVISION OF THE STEM, BIOLOX DELTA CERAMIC HEAD AND ECIMA INSERT AFTER APPROXIMATELY 4 MONTHS DUE TO LOOSE CEMENT MANTLE AND THIGH PAIN.
Patient problems: Pain
MAUDE report 23861814 ↗InjuryDec 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
TAPERFIT REVISION OF THE STEM AND CEMENT RESTRICTOR AFTER APPROXIMATELY 3 MONTHS DUE TO A PERI-PROSTHETIC FRACTURE FOLLOWING A FALL.
Patient problems: Bone Fracture(s)
MAUDE report 23825398 ↗InjurySep 11, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
TAPERFIT / TRINITY DUAL MOBILITY REVISION OF THE STEM, ECIMA INSERT AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 4 YEARS AND 6 MONTHS DUE TO A PERI-PROSTHETIC FRACTURE FOLLOWING A FALL.
Patient problems: Bone Fracture(s)
MAUDE report 23026296 ↗InjurySep 10, 2025Fracture; Fracture
TAPERFIT / TRINITY REVISION OF THE STEM AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 12 YEARS DUE TO FRACTURE OF THE STEM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23013641 ↗InjuryJun 2, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
TAPERFIT / TRINITY REVISION OF THE STEM, ECIMA INSERT AND MODULAR HEAD AFTER APPROXIMATELY 2 YEARS AND 1 MONTH DUE TO LOOSENING OF THE STEM (PATIENT HAD MULTIPLE FALLS).
Patient problems: Fall
MAUDE report 22126224 ↗InjuryJun 2, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
TAPERFIT / TRINITY REVISION OF THE STEM, CUP, ECIMA LINER, BIOLOX DELTA CERAMIC HEAD AND 2 SCREWS AFTER APPROXIMATELY 4 YEARS AND 10 MOTHS DUE TO IMPINGEMENT.
Patient problems: Joint Impingement
MAUDE report 22124072 ↗InjuryApr 29, 2025Fracture; Fracture
TAPERFIT / TRINITY REVISION OF THE STEM, SHELL, ECIMA LINER AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 6 YEARS AND 2 MONTHS DUE TO FRACTURE OF THE STEM. DURING THE REVISION IT WAS NOTED THAT THERE APPEARED TO BE INFECTION.
Patient problems: Unspecified Infection
MAUDE report 21924487 ↗InjuryNov 6, 2024Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
TAPERFIT / TRINITY REVISION OF THE STEM, COCR MODULAR HEAD AND HXLPE LINER AFTER APPROXIMATELY 9 YEARS AND 3 MONTHS DUE TO PAIN.
Patient problems: Pain
MAUDE report 20618596 ↗
Other Corin Ltd products
All Corin Ltd 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.
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