Trident 621-10-28DRecalls & reported problems
Howmedica Osteonics Corp. · 10 Degree Polyethylene Insert · Class 2 · Implant
All models of Trident (160)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613327037746), received between Feb 27, 2019 and Nov 17, 2022 — classified as 4 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Device Dislodged or Dislocated2
- Degraded1
- Insufficient Device Problem Information1
- Loss of Osseointegration1
Patient problems
- Injury3
- Joint Dislocation2
- Ambulation or Postural Difficulties1
- Inadequate Osseointegration1
- Unspecified Infection1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryNov 17, 2022Degraded; Loss of Osseointegration; Degraded; Loss of Osseointegration
IT WAS REPORTED BY THE SALES REP THAT THE SURGEON NOTIFY ON A POSSIBLE REMOVAL CASE DUE TO LOOSENING.
Patient problems: Ambulation or Postural Difficulties; Inadequate Osseointegration
MAUDE report 15812798 ↗InjuryApr 18, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
THIS PI IS FOR REVISION 1 DONE ON (B)(6) 2015 PATIENT HAD A RIGHT HIP REPLACEMENT DONE ON (B)(6) 2014. PATIENT WAS REVISED 3 TIMES DUE TO INFECTION AND OTHER COMPLICATIONS.
Patient problems: Injury; Unspecified Infection
MAUDE report 8526905 ↗InjuryFeb 27, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated
THIS PI IS FOR DISLOCATION AND CLOSED REDUCTION ON (B)(6) 2016. IT WAS REPORTED THROUGH THE FILING OF A LAWSUIT THAT ALLEGEDLY ON (B)(6) 2016 AND AGAIN ON (B)(6) 2016 THE PATIENT WAS ADMITTED FOR DISLOCATIONS AND UNDERWENT CLOSED REDUCTIONS OF THE HIP. IT IS FURTHER ALLEGED ON (B)(6) 2017 LESS THAN TWO MONTHS AFTER THE LAST CLOSED REDUCTION SHE WAS BACK IN THE HOSPITAL BECAUSE OF A DISLOCATION AND PAIN. THE CUP AND LINER WERE REMOVED AND REPLACED.
Patient problems: Injury; Joint Dislocation
MAUDE report 8375257 ↗InjuryFeb 27, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated
THIS PI IS FOR DISLOCATION AND CLOSED REDUCTION ON (B)(6) 2016. IT WAS REPORTED THROUGH THE FILING OF A LAWSUIT THAT ALLEGEDLY ON (B)(6) 2016 AND AGAIN ON (B)(6) 2016 THE PATIENT WAS ADMITTED FOR DISLOCATIONS AND UNDERWENT CLOSED REDUCTIONS OF THE HIP. IT IS FURTHER ALLEGED ON (B)(6) 2017 LESS THAN TWO MONTHS AFTER THE LAST CLOSED REDUCTION SHE WAS BACK IN THE HOSPITAL BECAUSE OF A DISLOCATION AND PAIN. THE CUP AND LINER WERE REMOVED AND REPLACED.
Patient problems: Injury; Joint Dislocation
MAUDE report 8375142 ↗
Other Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate devices
- Novation 130-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls156 reports
- Novation 130-36-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls79 reports
- CORAIL 3L92511Depuy (Ireland) · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate158 reports
- Acumatch A Series 138-36-29Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate3 recalls1 report
- Novation 136-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls43 reports
- Novation 130-32-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls33 reports
- Novation 132-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls26 reports
- Novation 136-36-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls22 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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