Trident 623-10-28ERecalls & reported problems
Howmedica Osteonics Corp. · 10 Degree Polyethylene Insert · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327039788), received between Jul 10, 2018 and Nov 13, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Degraded” (2 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
- Degraded2
- Naturally Worn1
Patient problems
- Injury1
- Joint Dislocation1
- Osteolysis1
- Tissue Damage1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryNov 13, 2023Degraded; Naturally Worn; Degraded; Naturally Worn
THE LINER WAS REPLACED DUE TO OSTEOLYSIS CAUSED BY LINER WEAR.
Patient problems: Osteolysis
MAUDE report 18117805 ↗InjuryJul 10, 2018Degraded; Degraded
REVISION OF LUXATED HIP REVEALED MASSIVE LOSS OF SOFT TISSUE AROUND GREATER TROCHANTER AND ACCOMPANYING PARTICLE DEBRIS AROUND THE SPIGOT, INSIDE THE HEAD TRUNNION AND IN THE WOUND AS A BLACK PATTERN. THE PRODUCTS REVISED WERE ACCOLADE TMZF WITH TRIDENT CUP. THE STEM, HEAD AND LINER WERE RETRIEVED AND AVAILABLE FOR FURTHER INSPECTION. AS TO MARKS ON THE STEM, THE SURGEON USED ONLY OSTEOTOME AROUND THE PROXIMAL PART OF THE FIXATION ZONE AND NOT ON THE TRUNNION. MARK ON THE HEAD ONLY ON THE OUTSIDE TO TAP OUT THE HEAD. THE STEM WAS WITHDRAWN WITH THE THREADED ACCOLADE2 INSERTER. NO OTHER MARKS WERE CAUSED BY USING OSTEOTOME OR OTHER INSTRUMENT.
Patient problems: Injury; Joint Dislocation; Tissue Damage
MAUDE report 7675322 ↗
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 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.
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