Trident 623-10-28CRecalls & 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
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327039771), received between Mar 7, 2022 and Dec 29, 2022 — classified as 3 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 reports).
2 other recalls cover devices cleared under the same FDA submission (K033716); they may or may not involve this specific model.
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.
Most reported problems
Device problems
- Device Dislodged or Dislocated3
- Unstable1
Patient problems
- Joint Dislocation3
- Joint Laxity1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryDec 29, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT HAD AN OPEN REDUCTION FOR DISLOCATION.
Patient problems: Joint Dislocation
MAUDE report 16068708 ↗InjuryDec 22, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED BY THE HEALTH PROFESSIONAL THAT THERE IS A REVISION FOR THR. REASON FOR REVISION DUE TO DISLOCATION.
Patient problems: Joint Dislocation
MAUDE report 16033642 ↗InjuryMar 7, 2022Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated
PATIENT HAD AN INDEX LEFT THA ON (B)(6) 2021. PATIENT PRESENTED WITH INSTABILITY AND DISLOCATION OF LEFT HIP. UNDERWENT REVISION FOR INSTABILITY ON (B)(6) 2021. CUP, LINER, AND HEAD WERE EXCHANGED.
Patient problems: Joint Dislocation; Joint Laxity
MAUDE report 13677947 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K033716. One submission often covers many models, so check the product and lot details in each record.
- Z-2810-2015 · Jun 25, 2015 · TerminatedTrident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component
- Z-0909-2010 · Feb 17, 2006 · TerminatedTrident Acetabular Hip System Polyethylene Inserts, Stryker Orthopaedics, multiple sizes, Mahwah, NJ. Intended for use in cementless fixation fro use in total hip arthroplasty to
Other Prosthesis, hip, semi-constrained, metal/polymer, uncemented devices
- LFIT 6260-9-136Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented166 reports
- Trident 623-00-36EHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented112 reports
- Accolade 6021-0435Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented88 reports
- EXETER 0580-1-044Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 recall22 reports
- Endo-Model SL Knee Prosthesis System 16-2840/02WALDEMAR LINK GmbH & Co. KG · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented1 recall17 reports
- Endo-Model SL Knee Prosthesis System 16-2840/05WALDEMAR LINK GmbH & Co. KG · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented1 recall12 reports
- Trident 623-10-36EHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented57 reports
- LFIT 6260-9-336Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented56 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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