Trinity-i Acetabular Shell 321.03.350Recalls & reported problems
Corin Ltd · Trinity-i Acetabular Shell Ø50mm Taper Size 3 · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 05055343870600), received between Jun 2, 2025 and Mar 31, 2026 — classified as 6 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (3 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, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information3
- Adverse Event Without Identified Device or Use Problem2
- Osseointegration Problem1
- Wrong Label1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Bone Fracture(s)1
- Inadequate Osseointegration1
- Joint Dislocation1
- Joint Laxity1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryMar 31, 2026Insufficient Device Problem Information
TRINITY REVISION (OPS USED IN PRIMARY) OF THE ECIMA LINER AND CUP AFTER APPROXIMATELY 1 YEAR DUE TO DISLOCATION.
Patient problems: Joint Dislocation
MAUDE report 24739408 ↗InjuryFeb 4, 2026Wrong Label
TRINITY SHELL INCORRECTLY LABELLED. THIS WAS IDENTIFIED PRIOR TO USE, HOWEVER, DID CAUSE SURGERY TO BE EXTENDED BY APPROXIMATELY 50 MINUTES. THERE HAS BEEN NO OTHER REPORTED SURGICAL OR PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24255799 ↗InjuryDec 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
TRINITY REVISION OF THE CUP, ECIMA LINER, 2 SCREWS AND BIOLOX DELTA CERAMIC HEAD AFTER 1 WEEK DUE TO A FRACTURE IN THE ACETABULUM AND A DISPLACED CUP.
Patient problems: Bone Fracture(s)
MAUDE report 23826002 ↗InjuryDec 9, 2025Osseointegration Problem; Osseointegration Problem
TRINITY REVISION AFTER APPROXIMATIVELY 2 YEARS AND 11 MONTHS DUE TO LOOSENING OF THE CUP AND POTENTIAL INFECTION.
Patient problems: Inadequate Osseointegration
MAUDE report 23755930 ↗InjuryNov 27, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
TRINITY REVISION AFTER APPROXIMATIVELY 10 MONTHS DUE TO MISPOSITIONING OF THE CUP DURING PRIMARY PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23664308 ↗InjuryJun 2, 2025Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
TRINITY DUAL MOBILITY REVISION OF THE CUP, COCR LINER, ECIMA INSERT AND BIOLOX DELTA CERAMIC HEAD AFTER APPROXIMATELY 5 YEARS AND 9 MONTHS DUE TO INSTABILITY.
Patient problems: Joint Laxity
MAUDE report 22126222 ↗
Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices
- BIOLOX DELTA 1365-32-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented551 reports
- PINNACLE ALTRX 1221-36-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented481 reports
- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
- BIOLOX DELTA 1365-36-720Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death189 reports
- DJO SURGICAL 400-03-362Encore Medical, L.P. · Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented187 reports
- Anthology 71365705Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented176 reports
- BIOLOX DELTA 1365-40-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented170 reports
- PINNACLE GRIPTION 1217-32-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented169 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 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