Trident 502-01-48DRecalls & reported problems
Howmedica Osteonics Corp. · Hemispherical Acetabular Shell · Class 2 · Implant
All models of Trident (160)
Data updated Oct 16, 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 07613153073062), received between Mar 2, 2018 and May 6, 2019 — classified as 2 injuries.
The most frequently reported specific device problem is “Loss of Osseointegration” (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
- Loss of Osseointegration1
- Osseointegration Problem1
Patient problems
- Inadequate Osseointegration2
- Injury2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 6, 2019Osseointegration Problem; Osseointegration Problem
IT WAS REPORTED THAT,"THE PATIENT ALLEGES FAILURE OF HIS HIP PROSTHESIS." "ON (B)(6) 2009 A REVISION OF THE LEFT TOTAL HIP ARTHROPLASTY WAS PERFORMED..."[...] A DIAGNOSIS OF LOOSENING LEFT TOTAL HIP ARTHROPLASTY ACETABULAR AND FEMORAL COMPONENTS WAS NOTED. THERE WAS NO EVIDENCE OF INFECTION AND THE CUP WAS GROSSLY LOOSE." EVENT UPDATE: [...] "THE FEMORAL PEDESTAL WAS NOTED DISTALLY AND FLEXIBLE REAMERS WERE ATTEMPTED TO BYPASS THIS DURING THE REVISION, DURING WHICH TIME IT EXITED POSTERIORLY OUT THE FEMUR. IT WAS SUBSEQUENTLY SUCCESSFULLY REAMED PAST THE PEDESTAL. A FRACTURE OF THE PROXIMAL LATERAL FEMUR WAS NOTED DURING THE SURGERY, WHICH WAS FIXED WITH A 2MM DALL-MILES CABLE. A SECUR-FIT PLUS STEM WAS IMPACTED WITH "SECURE FIXATION".
Patient problems: Inadequate Osseointegration; Injury
MAUDE report 8583619 ↗InjuryMar 2, 2018Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED PATIENT'S HIP WAS REVISED DUE TO SHELL LOOSENING. REP WAS NOT PRESENT FOR THE PROCEDURE.
Patient problems: Inadequate Osseointegration; Injury
MAUDE report 7309518 ↗
Other Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented devices
- STAGEONE 431209Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented2 recalls0 reports
- SELF CENTERING 1035-45-000Depuy Orthopaedics, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented84 reports
- LFIT 6260-9-036Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented80 reports
- ACTIS 101011060Depuy (Ireland) · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented66 reports
- RINGLOC BI-POLAR HIP SYSTEM 11-165228Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall1 death12 reports
- SELF CENTERING 1035-44-000Depuy Orthopaedics, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented60 reports
- TANDEM 71324046Smith & Nephew, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall9 reports
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145170Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented59 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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