Trident 623-00-32FRecalls & reported problems
Howmedica Osteonics Corp. · 0 Degree Polyethylene Insert · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613327039474), received between Jul 25, 2018 and Oct 21, 2025 — classified as 2 injuries, 2 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated1
- Difficult to Insert1
- Fitting Problem1
- Insufficient Device Problem Information1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
- Unspecified Infection1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryOct 21, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
RE-OPERATION DUE TO DISLOCATION (REPLACEMENT OF LINER AND HEAD).
Patient problems: Insufficient Information
MAUDE report 23346238 ↗MalfunctionOct 9, 2020Difficult to Insert; Difficult to Insert
THE DR TRIED TO LOCK THE 32MM F 0DEG HIP INSERT IN AND IT WOULDN¿T ¿LOCK¿. HE REMOVED IT TO MAKE SURE THE SCREW HEAD WAS DOWN IN THE CUP AND THAT THERE WAS NOT AND SOFT TISSUE KEEPING IT FROM LOCKING. HE REMOVED AND TRIED 3 TIMES. WE THEN OPENED A NEW F INSERT AND IT LOCKED IMMEDIATELY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10654905 ↗MalfunctionNov 20, 2018Fitting Problem; Fitting Problem
AFTER IMPLANTING TRIDENT CUP INTO THE PATIENT, INSERT X3 LINER. THIS FAILS AFTER SEVERAL ATTEMPTS AND IT IS BELIEVED THAT THE SIZE IS INCORRECT. ONE OPENS A NEW PACKAGE OF THE SAME SIZE AND FITS DIRECTLY. 5-10 MINUTES DELAY IN SURGERY DUE TO THIS FAILURE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8090376 ↗InjuryJul 25, 2018Insufficient Device Problem Information; Insufficient Device Problem Information
THE CUSTOMER QUERIED EXPIRY DATES OF 3 DEVICES WHICH HAD BEEN IMPLANTED INTO A PATIENT. THE PATIENT HAS EXPERIENCED AN UNSPECIFIED EVENT. UPDATE: THE CUSTOMER REPORTS THAT THE PATIENT'S JOINT IS INFECTED; THE CUSTOMER HAS REQUEST EXPIRE DATE OF THE DEVICES.
Patient problems: Unspecified Infection
MAUDE report 7718478 ↗
Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices
- BIOLOX DELTA 1365-32-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented551 reports
- PINNACLE ALTRX 1221-36-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented481 reports
- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
- BIOLOX DELTA 1365-36-720Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death189 reports
- DJO SURGICAL 400-03-362Encore Medical, L.P. · Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented187 reports
- Anthology 71365705Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented176 reports
- BIOLOX DELTA 1365-40-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented170 reports
- PINNACLE GRIPTION 1217-32-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented169 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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