Trident 623-10-36GRecalls & reported problems

Summary

The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 07613327039931), received between May 31, 2017 and Jul 8, 2026 — classified as 13 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 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

Recent adverse event reports

The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.

• InjuryJul 8, 2026Adverse Event Without Identified Device or Use Problem

  THE FOLLOWING INFORMATION WAS PROVIDED: BOOKED KIT FOR REVISION OF HEAD AND LINER. PT NEEDS REVISION OF LINER SO HEAD AND LINER PLANNED TO BE EXCHANGED.

  Patient problems: Insufficient Information

  MAUDE report 25757067 ↗
• InjuryMar 19, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT WAS REVISED ON (B)(6) 2024 DUE TO DISLOCATION. SPOKE TO REP. REP CONFIRMED THE HEAD CAME OUT OF THE LINER. REP ALSO CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Joint Dislocation

  MAUDE report 18936897 ↗
• InjuryJun 22, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED DUE TO DISLOCATION OF THE HEAD FROM THE LINER. HEAD AND LINER WERE REVISED TO ANOTHER HEAD, MDM METAL LINER, AND ADM/ MDM POLY INSERT. REP PROVIDED PRIMARY USAGE AND MAY BE ABLE TO CONFIRM THE DATE OF REVISION AND PROVIDE REVISION USAGE. OTHERWISE, REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Joint Dislocation

  MAUDE report 14778598 ↗
• InjuryMar 27, 2022Degraded; Naturally Worn; Degraded; Naturally Worn

  ORIGINAL TOTAL HIP REPLACEMENT (B)(6) 2010 PATIENT HAD ACETABULAR COMPONENTS AND FEMORAL HEAD REMOVED AND REPLACED WITH TRITANIUM SHELL AND MDM LINER SURGEON RECORDED OSTEOLYSIS AS REASON FOR REVISION ON JOINT REGISTRY FORM. LEFT SIDE.

  Patient problems: Osteolysis

  MAUDE report 13925277 ↗
• InjuryOct 20, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED DUE TO INFECTION. SURGEON PERFORMED A WASHOUT AND HEAD AND LINER EXCHANGE. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Unspecified Infection

  MAUDE report 12665786 ↗
• InjuryFeb 16, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REMOVAL OF RESTORATION MODULAR AND PSL SHELL AND LINER DUE TO WOUND INFECTION. ORIGINAL SURGERY FROM 2015. REPLACED WITH CEMENT SPACER.

  Patient problems: Unspecified Infection

  MAUDE report 11333307 ↗
• InjuryOct 9, 2020Naturally Worn; Naturally Worn

  FIRST SURGERY ON (B)(6) 2013. LEFT HIP THA. FROM HALF A YEAR AGO, THERE WAS A POSSIBILITY OF OSTEOLYSIS DUE TO POLYETHYLENE WEAR ON THE SLIDING SURFACE OF THE LINER AND HEAD. DUE TO THE LUCENT LINE FINDINGS IN THE PROXIMAL FEMUR, THE REVISION WAS IMPLEMENTED ON (B)(6) 2020. PER SALES REP: THE REMOVED IMPLANT HAS SOME SCRATCHES ON BOTH THE POLYETHYLENE AND THE HEAD, BUT IT IS HARD TO SAY THAT IT LED TO THIS REVISION DUE TO 100% OSTEOLYSIS. A LARGE NUMBER OF HEMATOMAS WERE FOUND IN THE WOUND, WHICH MAY HAVE CAUSED THE HEMATOMA TO ENTER THE SLIDING SURFACE, CAUSING SCRATCHES AND WEAR OF POLYETHYLENE.

  Patient problems: Hematoma; Osteolysis

  MAUDE report 10654509 ↗
• InjuryDec 5, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  OUR LEGAL DEPARTEMENT REPORTED A CLAIM BY THE LAWYER OF A PATIENT IMPLANTED WITH A TRIDENT, HIPSTAR AND V40 HEAD AT HOSPITAL ON (B)(6) 2009. PRODUCTS INVOLVED SEEM TO BE TRIDENT, HIPSTAR AND V40 HEAD. THE CLAIM STATES THAT THE PATIENT UNDERWENT A REVISION SURGERY DUE TO DISLOCATION OF THE HEAD.

  Patient problems: Joint Dislocation

  MAUDE report 9419041 ↗
• MalfunctionApr 1, 2019Fitting Problem; Fitting Problem

  IT WAS REPORTED THAT THE X3 POLY FIT INSIDE THE TRIDENT ACETABULAR CUP, HOWEVER THE POLY WAS CONSISTENTLY MOVING AND DID NOT SNAP INTO THE CUP. AS A RESULT, THE POLY WOULD NOT STOP ROTATING AND WAS NOT ABLE TO BE IMPLANTED. A NEW POLY OF THE SAME SIZE WAS OPENED, WHICH FIT THE CUP, AND THE SURGERY WAS COMPLETED WITHOUT FURTHER INCIDENT. IT WAS REPORTED THAT A SURGICAL DELAY OF 5 MINUTES OCCURRED (SPENT SEATING THE POLY).

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8471858 ↗
• InjuryJan 14, 2019Difficult to Insert; Difficult to Insert

  SURGEON TRIED TO FIT A TRIDENT 10 DEGREE LINER (X3) INTO TRIDENT CUP. WOULD NOT SIT, REGARDLESS OF TROUBLESHOOTING. NEW LINER SAT PERFECTLY FIRST TIME.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8245315 ↗
• InjuryMar 8, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  THE SOLICITOR'S LETTER INDICATED THAT THE PATIENT WAS IMPLANTED WITH A STRYKER RIGHT THR FOLLOWING REVISION SURGERY ON (B)(6) 2014. ON (B)(6), THE PATIENT WAS REVIEWED AND MRI SCAN SHOWED CHRONIC INFECTION AROUND THE RIGHT HIP REPLACEMENT SUGGESTING DEEP INFECTION. THE PATIENT UNDERWENT FIRST STAGE REVISION SURGERY ON (B)(6) 2015. THE PATIENT REMAINED WITHOUT A HIP JOINT WHILE HE WAS TREATED WITH ANTIBIOTICS FOR 6 WEEKS. THE PATIENT UNDERWENT SECOND STAGE (THR) SURGERY IN 2016.

  Patient problems: Injury; Unspecified Infection

  MAUDE report 7324379 ↗
• InjuryDec 27, 2017Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

  REVISION CASE. HEAD AND LINER AND SCREW WERE REMOVED. NEW HEAD AND LINER INSERTED. RIGHT HIP.

  Patient problems: Injury; Insufficient Information

  MAUDE report 7147768 ↗
• InjuryDec 12, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT SURGEON PERFORMED A STAGE 1 REVISION ON PATIENT'S RIGHT HIP DUE TO INFECTION (INFECTION CLINICALLY CONFIRMED, MICROORGANISM NOT REPORTED TO REP). A STEM AND SHELL WHICH WERE IMPLANTED IN 2008, AND A HEAD AND INSERT WHICH WERE IMPLANTED IN 2016 WERE ALL EXPLANTED.

  Patient problems: Injury; Unspecified Infection

  MAUDE report 7110536 ↗
• MalfunctionJun 9, 2017Fitting Problem; Material Deformation; Material Distortion; Material Distortion

  THE SURGEON REPORTED THAT HE ATTEMPTED TO IMPACT THE LINER INTO THE ACETABULUM CUP WHICH HE HAD JUST PLACED INTO THE PELVIS. ON IMPACTION (WITH THE CORRECT LINER IMPACTOR) THE LINER FAILED TO SEAT CORRECTLY INTO THE CUP. THE SURGEON REMOVED THE LINER TO EXAMINE THE PROBLEM MORE CLOSELY. ON FURTHER INSPECTION, THE SURGEON NOTICED THE FOUR INDEXING BARBS WHICH ARE CIRCUMFERENTIALLY ALIGNED AROUND THE RIM OF THE POLYETHYLENE LINER WERE NOT FULLY FORMED. FOLLOWING THIS, THE LINER WAS PLACED ASIDE AND NOT USED. SUBSEQUENTLY, A DIFFERENT LINER WAS OPENED AND IMPLANTED INTO THE PATIENT. NO HARM WAS CAUSED TO THE PATIENT FROM THE FAULTY IMPLANT. THERE WAS A SHORT SURGICAL DELAY OF 3 MINUTES WHILE A NEW LINER WAS OPENED.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 6632148 ↗
• InjuryMay 31, 2017Insufficient Device Problem Information; Insufficient Device Problem Information

  SALES REP REPORTED A LEFT HIP REVISION STATING LINER WASN'T SEATED AND LEG LENGTH DISCREPANCY PRESENT. LINER WAS REMOVED AND REPLACED, SHORTER HEAD/NECK WAS ALSO REPLACED.

  Patient problems: Injury

  MAUDE report 6603040 ↗