Trident 540-11-60GRecalls & reported problems
Howmedica Osteonics Corp. · Solid Back Acetabular Shell · Class 2 · Implant
All models of Trident (160)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540237873), received between Jun 12, 2023 and Jun 12, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Positioning Problem” (1 report).
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 16, 2026.
Most reported problems
Device problems
- Positioning Problem1
Patient problems
- Ambulation or Postural Difficulties1
- Bone Fracture(s)1
- Extraskeletal ossification1
- Joint Laxity1
- Muscle/Tendon Damage1
- Osteolysis1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 12, 2023Positioning Problem; Positioning Problem
WIFE REPORTED HER HUSBAND HAD A REVISION OF THE LEFT HIP ON (B)(6) 2022 DUE TO THE "TWO METALS BEING WORN DOWN TO FINE PENCIL TIPS". PRIMARY SURGERY WAS DONE IN (B)(6) 2007. UPDATE: PER PATIENT MEDICAL RECORDS, IT WAS INDICATED THAT THE PATIENT WAS REVISED DUE TO DISASSOCIATION OF THE HEAD FROM THE STEM, FRACTURE OF THE FEMORAL STEM TRUNNION, METALLOSIS AND OSTEOLYSIS, DESTRUCTION OF ABDUCTORS, HETEROTOPIC OSSIFICATION AND FRACTURE OF THE GREATER TROCHANTER WHEREBY THE STEM, HEAD AND LINER WERE EXPLANTED AND THE PATIENT WAS CONVERTED TO A RESTORATION MODULAR CONSTRUCT WITH DALL MILES GRIP PLATE AND CABLING FOR FIXATION. IT WAS ALSO REPORTED THAT THE SHELL WAS SLIGHTLY MORE VERTICAL THAN IDEAL BUT REMOVAL WOULD HAVE CAUSED SIGNIFICANT BONE LOSS, SO IT WAS LEFT IMPLANTED. DURING REVISION SURGERY, THE FOLLOWING WERE PERFORMED: "DEBRIDEMENT OF CHRONIC METALLIC WEAR DEBRIS AND OSTEOLYSIS," "OPEN REDUCTION INTERNAL FIXATION LEFT GREATER TROCHANTER FRACTURE," AND "RESECTION OF HETEROTOPIC OSSIFICATION." DESPITE THE REPORTED PROXIMAL BONE EROSIONS, THE FEMORAL STEM WAS REPORTED TO BE WELL-FIXED AND REMOVAL WAS INTENSIVE.
Patient problems: Ambulation or Postural Difficulties; Bone Fracture(s); Extraskeletal ossification; Joint Laxity; Muscle/Tendon Damage; Osteolysis; Pain
MAUDE report 17103250 ↗
Other Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous devices
- Accolade 6021-0537Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous46 reports
- PROFEMUR® PHAC1252Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous37 reports
- Accolade 6020-0335Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous35 reports
- OXINIUM 71342340Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous32 reports
- EXETER 0580-1-351Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous29 reports
- INSTRUMENT 2101-0200Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous27 reports
- REFLECTION 71330001Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous20 reports
- Accolade 6720-0330Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous18 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
- 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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