Trinity Acetabular Hip SystemRecalls & reported problems across all models
Corin Ltd · 12 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 21
- Deaths reported
- 0
- Injuries reported
- 21
- Recalls
- 0
We found 12 models of Trinity Acetabular Hip System by Corin Ltd in the FDA's device registry (GUDID). Together they are named in 21 adverse event reports in the FDA's MAUDE database, received between Jul 11, 2025 and Sep 22, 2026 — classified as 21 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (5 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 Trinity Acetabular Hip System problems
Device problems
- Adverse Event Without Identified Device or Use Problem17
- Insufficient Device Problem Information5
- Compatibility Problem1
- Loss of Osseointegration1
- Mechanical Problem1
Patient problems
- Unspecified Infection10
- Joint Laxity3
- Joint Dislocation2
- Joint Impingement2
- Metal Related Pathology2
- Bone Fracture(s)1
- High metal ion levels1
- No Clinical Signs, Symptoms or Conditions1
Trinity Acetabular Hip System models
12 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Trinity Acetabular Hip System 321.03.352Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- Trinity Acetabular Hip System 325.03.040Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented4 reports
- Trinity Acetabular Hip System 321.03.536Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- Trinity Acetabular Hip System 325.04.042Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate2 reports
- Trinity Acetabular Hip System 325.05.045Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- Trinity Acetabular Hip System 321.02.348Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Trinity Acetabular Hip System 321.05.362Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 report
- Trinity Acetabular Hip System E321.128Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Trinity Acetabular Hip System E321.232Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Trinity Acetabular Hip System 321.02.532Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Trinity Acetabular Hip System 321.04.540Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Trinity Acetabular Hip System 321.05.540Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
Recent Trinity Acetabular Hip System adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 22, 2026Adverse Event Without Identified Device or Use Problem
Trinity Dual Mobility and Paragon revision (with OPS used in primary surgery) of all devices after approximatively 3 weeks due to infection.Note: the Paragon stem GM08001-203-03 is not cleared in the USA.
Patient problems: Unspecified Infection
MAUDE report 50851396 ↗InjurySep 17, 2026Adverse Event Without Identified Device or Use Problem
Trinity Dual Mobility revision (with OPS used at primary) of the CoCr Liner, ECiMa Insert and BIOLOX Delta Ceramic Head after approximately 1 year and 1 month as the patient was impinging.
Patient problems: Joint Impingement
MAUDE report 50803862 ↗InjurySep 14, 2026Adverse Event Without Identified Device or Use Problem
Trinity Dual Mobility revision of the Cup, CoCr Liner and ECiMa Insert after approximately 1 month due to infection.Please note: this is the 2nd revision for this patient. A previous revision was performed and reported under reference 9614209-2025-00635.
Patient problems: Unspecified Infection
MAUDE report 50753891 ↗InjurySep 14, 2026Insufficient Device Problem Information
Trinity Dual Mobility revision of the CoCr Liner and ECiMa Insert after approximatively 11 months due to metallosis.
Patient problems: Metal Related Pathology
MAUDE report 50751897 ↗InjuryJul 9, 2026Adverse Event Without Identified Device or Use Problem
TRINITY DUAL MOBILITY (OPS USED IN PRIMARY) REVISION OF THE COCR LINER, ECIMA INSERT AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 1 YEAR AND 11 MONTHS DUE TO INFECTION WITH SUSPICION OF METALLOSIS. NOTE: LATE REPORT DUE TO THE REPORTER INFORMING VIGILANCE LATE. REPORTER MADE AWARE ON (B)(6) 2026 BUT DID NOT SUBMIT TO VIGILANCE UNTIL (B)(6) 2026.
Patient problems: Unspecified Infection
MAUDE report 25764003 ↗InjuryJun 18, 2026Mechanical Problem
TRINITY/TRINITY DUAL MOBILITY REVISION OF THE CLUSTER SHELL, BIOLOX DELTA CERAMIC MODULAR HEAD AND ECIMA INSERT AFTER APPROXIMATIVELY 3 YEARS AND 2 MONTHS DUE TO IMPINGEMENT.
Patient problems: Joint Impingement
MAUDE report 25545029 ↗InjuryApr 23, 2026Adverse Event Without Identified Device or Use Problem
MOBILIT AND TRINITY REVISION OF THE POLYETHYLENE INSERT AND COCR MOD HEAD AFTER 1 MONTH DUE TO INFECTION. NOTE 1: THE MOBILIT INSERT HDM250 IS NOT CLEARED IN THE USA. NOTE 2: THIS IS A REGULARIZATION WITHIN THE FRAMEWORK OF A CLINICAL STUDY FOLLOWING A CHANGE IN OUR EVENT MONITORING PROCESS OF SAE FROM CLINICAL STUDY.
Patient problems: Unspecified Infection
MAUDE report 24965861 ↗InjuryFeb 4, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
TRINITY REVISION OF THE ECIMA LINER AND MODULAR HEAD AFTER APPROXIMATELY 9 YEARS, 5 MONTHS AND 2 WEEKS DUE TO INSTABILITY AND DISLOCATION.
Patient problems: Joint Laxity
MAUDE report 24258742 ↗InjuryFeb 4, 2026Loss of Osseointegration
TRINITY REVISION OF CUP, ECIMA LINER, BIOLOX DELTA MOD HEAD AND SCREW AFTER 2 MONTHS DUE TO CUP SUBSIDING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24258454 ↗InjuryFeb 3, 2026Adverse Event Without Identified Device or Use Problem
TRINITY REVISION AFTER APPROXIMATIVELY 3 MONTHS DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 24246246 ↗InjuryDec 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
TRINITY DUAL MOBILITY REVISION OF THE COCR LINER, ECIMA INSERT AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 1 MONTH DUE TO PAIN, INFLAMMATION AND INFECTION.
Patient problems: Unspecified Infection
MAUDE report 23862892 ↗InjuryDec 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
TRINITY DUAL MOBILITY REVISION OF THE ECIMA INSERT AND COCR LINER AFTER APPROXIMATELY 2 YEARS AND 4 MONTHS DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 23861713 ↗InjuryNov 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
METAFIX COLLARED / TRINITY REVISION OF THE COLLARED STEM, CUP, ECIMA LINER AND CERAMIC HEAD AFTER NEARLY 4 WEEKS DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 23592349 ↗InjuryNov 3, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
TRINITY DUAL MOBILITY REVISION OF THE CUP, SCREW, COCR LINER, ECIMA INSERT AND MODULAR HEAD AFTER APPROXIMATELY 2 YEARS DUE TO CUP LOOSENING AND IMPINGEMENT.
Patient problems: Joint Laxity
MAUDE report 23451609 ↗InjuryOct 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
TRINITY AND METAFIX REVISION OF ALL PARTS AFTER APPROXIMATIVELY 1 MONTH DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 23265272 ↗
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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