TaperFit Cemented Hip System 588.3800Recalls & reported problems
Corin Ltd · TaperFit Hip Stem 38mm Offset Narrow Stem size 0 · Class 2 · Implant
All models of TaperFit Cemented Hip System (8)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05055343871065), received between Jun 2, 2025 and Sep 10, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (1 report).
1 FDA recall record name this device's 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Recalls naming this device
- Jul 12, 2022Class IITerminated
Some of the devices did not pass fatigue testing.
Z-1667-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Fracture1
- Insufficient Device Problem Information1
Patient problems
- Joint Impingement1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
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, 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 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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