Trinity Acetabular Hip System with ECiMa LinersRecalls & reported problems across all models
Corin Ltd · 9 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 28
- Deaths reported
- 0
- Injuries reported
- 28
- Recalls
- 0
We found 9 models of Trinity Acetabular Hip System with ECiMa Liners by Corin Ltd in the FDA's device registry (GUDID). Together they are named in 28 adverse event reports in the FDA's MAUDE database, received between Dec 7, 2022 and Sep 30, 2026 — classified as 28 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (4 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 with ECiMa Liners problems
Device problems
- Adverse Event Without Identified Device or Use Problem23
- Insufficient Device Problem Information4
- Device Dislodged or Dislocated1
- Fracture1
- Loss of Osseointegration1
- Osseointegration Problem1
Patient problems
- Unspecified Infection15
- Joint Dislocation8
- Joint Laxity2
- Inadequate Osseointegration1
- No Clinical Signs, Symptoms or Conditions1
- Skin Inflammation/ Irritation1
Trinity Acetabular Hip System with ECiMa Liners models
9 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Trinity Acetabular Hip System with ECiMa Liners 322.04.636Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented9 reports
- Trinity Acetabular Hip System with ECiMa Liners 322.03.636Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented6 reports
- Trinity Acetabular Hip System with ECiMa Liners 322.02.632Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate3 reports
- Trinity Acetabular Hip System with ECiMa Liners 322.04.640Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate2 reports
- Trinity Acetabular Hip System with ECiMa Liners 322.03.932Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- Trinity Acetabular Hip System with ECiMa Liners 322.04.936Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented2 reports
- Trinity Acetabular Hip System with ECiMa Liners 322.04.940Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate2 reports
- Trinity Acetabular Hip System with ECiMa Liners 322.05.740Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented1 report
- Trinity Acetabular Hip System with ECiMa Liners 322.02.932Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented1 report
Recent Trinity Acetabular Hip System with ECiMa Liners adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Adverse Event Without Identified Device or Use Problem
Trinity / MetaFix Collared revision of the Cup, 2 Screws, ECiMa Liner, BIOLOX Delta Ceramic Head and Collared Stem after approximately 2 years and 7 months due to infection.Note: the Metafix Stem 579.2101 is not cleared in the USA.
Patient problems: Unspecified Infection
MAUDE report 50942691 ↗InjuryAug 26, 2026Adverse Event Without Identified Device or Use Problem
TaperFit / Trinity revision of all components after nearly 8 months due to infection.
Patient problems: Unspecified Infection
MAUDE report 50447777 ↗InjuryAug 7, 2026Adverse Event Without Identified Device or Use Problem
Trinity revision (OPS used in primary) of ECiMa Liner after approx. 5 months due to dislocation.
Patient problems: Joint Dislocation
MAUDE report 50171412 ↗InjuryJul 29, 2026Adverse Event Without Identified Device or Use Problem
Trinity revision (OPS used in primary) of the ECiMa Liner after approximately 1 year and 9 months due to dislocation.
Patient problems: Joint Dislocation
MAUDE report 50070008 ↗InjuryJul 27, 2026Adverse Event Without Identified Device or Use Problem
Trinity revision of the ECiMa Liner after approximately 11 months due to dislocation.
Patient problems: Joint Dislocation
MAUDE report 50037746 ↗InjuryMay 27, 2026Adverse Event Without Identified Device or Use Problem
TRINITY REVISION OF THE ECIMA LINER AFTER 5 MONTHS DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 25299119 ↗InjuryMar 31, 2026Adverse Event Without Identified Device or Use Problem
TRINITY REVISION OF THE ECIMA LINER AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 8 YEARS AND 10 MONTHS DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 24739282 ↗InjuryMar 30, 2026Loss of Osseointegration; Osseointegration Problem
TRINITY REVISION (OPS USED IN PRIMARY) OF THE ECIMA LINER AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 4 MONTHS DUE TO LOOSENING.
Patient problems: Inadequate Osseointegration
MAUDE report 24713170 ↗InjuryMar 24, 2026Adverse Event Without Identified Device or Use Problem
TRINITY REVISION OF THE LINER AND HEAD AFTER APPROXIMATIVELY 2 WEEKS DUE TO INFECTION.NOTE 1: THIS REPORT IS UPDATED AS THE CUP REMAINED IN SITU. ONLY THE LINER AND THE HEAD WERE REVISED.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 24680780 ↗InjuryMar 12, 2026Fracture
TRINITY REVISION OF THE CUP, ECIMA LINER, BIOLOX DELTA CERAMIC HEAD AND SCREW AFTER APPROXIMATELY 1 YEAR AND 6 MONTHS. THE ECIMA LINER WAS LOOSE AND HAD FRACTURED THROUGH THE POSTERIOR RIM AND EPW JUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24579301 ↗InjuryJan 26, 2026Adverse Event Without Identified Device or Use Problem
TRINITY/ METAFIX REVISION OF ECIMA LINER, BIOLOX DELTA CERAMIC HEAD AND STEM AFTER 2.5 WEEKS DUE TO INFECTION AND DISLOCATION.
Patient problems: Unspecified Infection
MAUDE report 24178507 ↗InjuryJan 8, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
TRINITY REVISION OF THE ECIMA LINER AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 1 MONTH DUE TO DISLOCATION.
Patient problems: Joint Dislocation
MAUDE report 24000847 ↗InjuryDec 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
TRINITY REVISION OF THE ECIMA LINER AFTER APPROXIMATELY 3 YEARS AND 7 MONTHS DUE TO INSTABILITY.
Patient problems: Joint Laxity
MAUDE report 23826218 ↗InjuryNov 27, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
TRINITY REVISION OF THE CUP, ECIMA LINER, BIOLOX DELTA CERAMIC HEAD AND 2 SCREWS AFTER 16 DAYS DUE TO DISLOCATION AND POTENTIAL INFECTION.
Patient problems: Unspecified Infection
MAUDE report 23664155 ↗InjuryNov 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
TRINITY REVISION AFTER APPROXIMATIVELY 9 MONTHS DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 23567194 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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