Trident 500-01-62GRecalls & 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
- 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 07613153072966), received between Mar 29, 2022 and Mar 29, 2022 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Ambulation or Postural Difficulties1
- Inadequate Osseointegration1
- Osteolysis1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 29, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THROUGH THE FILING OF A LAWSUIT THAT ALLEGEDLY THE PATIENT WAS IMPLANTED WITH AN LIFT ANATOMIC COCR V40 FEMORAL HEAD ON HIS RIGHT HIP ON OR ABOUT (B)(6) 2007 AND WAS REVISED ON (B)(6) 2020. IT IS FURTHER ALLEGED THAT HE SUFFERED INJURIES AS A RESULT OF IMPLANTATION AND EXPLANTATION OF THE DEVICES AT ISSUE, DEVICE RECALL AND EXCESSIVE LEVELS OF CHROMIUM AND COBALT IN HIS BLOOD. UPDATE ON 03-MAR-2022 PER CLINICIAN REVIEW: "[...] AN OPERATIVE NOTE BY DR. DATED (B)(6) 2020 IS PROVIDED. THE PREOPERATIVE DIAGNOSIS WAS ¿MECHANICAL LOOSENING OF PROSTHETIC HIP¿ AND THE POSTOP DIAGNOSIS WAS THE SAME. THE OPERATION PERFORMED WAS A REVISION RIGHT TOTAL HIP ARTHROPLASTY. THE SURGEON USED A CEMENTLESS 70 MM SHELL, A POLYETHYLENE WITH A 28 MM INNER DIAMETER, A WAGNER SL FEMORAL STEM WAS UTILIZED, DEMINERALIZED BONE PUTTY, AND A 28 MM FEMORAL HEAD WAS UTILIZED. FEMORAL COMPONENT WAS GROSSLY LOOSE. THERE WAS NO EVIDENCE OF INFECTION. THE SURGEON DESCRIBES A HUGE AMOUNT OF OSTEOLYSIS WITH "AMORPHOUS SLUDGE TYPE OF WHITISH GRAY MATERIAL". HE STATES THAT THE FEMORAL HEAD WAS DISASSOCIATED FROM THE FEMORAL STEM AND THERE WAS A LARGE AMOUNT OF CORROSIVE BLACK TYPICAL MATERIAL ON BOTH THE
Patient problems: Ambulation or Postural Difficulties; Inadequate Osseointegration; Osteolysis
MAUDE report 13937767 ↗
Other Prosthesis, hip, hemi-, femoral, metal devices
- UHR UH1-48-28Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal2 recalls3 reports
- "UNITED" USTAR II Knee System 2515-3111United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- "UNITED" USTAR II Knee System 2515-3213United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- STAGEONE 431207Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal2 recalls0 reports
- "UNITED" USTAR II Knee System 2515-3115United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- ACTIS 101011050Depuy (Ireland) · Prosthesis, hip, hemi-, femoral, metal73 reports
- UHR UH1-46-26Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal1 recall11 reports
- UHR UH1-45-26Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal1 recall11 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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