Trident 623-00-36HRecalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07613327039559), received between Oct 19, 2018 and Apr 29, 2022 — classified as 6 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

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryApr 29, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IN PROVIDING INFORMATION FOR A REVISION OF THE PATIENT'S LEFT HIP ON (B)(6) 2022, REP PROVIDED USAGE SHEETS FOR (B)(6) 2020. COMPARING THEM, A TRIDENT LINER WAS REVISED TO AN MDM METAL LINER AND ADM/ MDM POLY INSERT, 4 SCREWS ADDED TO THE IN SITU SHELL, AND A RESTORATION MODULAR STEM CONSTRUCT WITH A CERAMIC FEMORAL HEAD WERE IMPLANTED. THIS REPORT IS FOR THE (B)(6) 2020 REVISION.

  Patient problems: Insufficient Information

  MAUDE report 14250498 ↗
• InjuryAug 7, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED. A 36 MM 'H' TRIDENT X3 0° POLY INSERT, V-40/C-TAPER ADAPTER SLEEVE, AND 36 +5 MM BIOLOX DELTA CERAMIC C-TAPER HEAD WERE REVISED TO A 44 MM 'H' TRIDENT X3 0° POLY INSERT, +4 MM UNIVERSAL V40 TAPER ADAPTER SLEEVE, AND A 44 MM BIOLOX DELTA ANATOMIC UNIVERSAL TAPER HEAD. "PATIENT HAS A CHRONIC INFECTION. LOW-ACTIVITY LEVEL, SEVERE BONE LOSS, COMPONENTS WERE EXCHANGED TO BEST TREAT THE INFECTION."

  Patient problems: Injury; Unspecified Infection

  MAUDE report 10378312 ↗
• InjuryJun 16, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

  ON (B)(6) 2014: RIGHT HIP REPLACEMENT, ON (B)(6) 2014: DISLOCATION RIGHT HIP, ON (B)(6) 2019: DISLOCATION RIGHT HIP, ON (B)(6) 2020: DISLOCATION RIGHT HIP; REVISION SURGERY IS PLANNED.

  Patient problems: Injury; Joint Dislocation

  MAUDE report 10157130 ↗
• InjuryNov 27, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  ON (B)(6) 2014 : TOTAL HIP REPLACEMENT IN HS038 REGISTRY, GOOD OUTCOME.(B)(6) 2019 : DISLOCATION OF THE HIP, REPOSITIONED THE SAME DAY. DEVICE NOT EXPLANTED.

  Patient problems: Ambulation or Postural Difficulties; Injury; Joint Dislocation

  MAUDE report 9385510 ↗
• InjuryNov 8, 2019Degraded; Noise, Audible; Degraded; Noise, Audible

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED. PRE-REVISION PATIENT COMPLAINT INCLUDED HEARING A POPPING SOUND. INTRA-OPERATIVELY, THE FOLLOWING WERE NOTED: TRUNNION WEAR, TRUNNION BROKE OFF THE STEM, GRAYISH BLACK TISSUE, WEAR OF THE LINER'S RIM DUE TO IMPINGEMENT OF THE STEM ON THE LINER. THE SHELL HAD NO ALLEGATIONS AGAINST IT AND WAS NOT REVISED. PATIENT WAS REVISED TO A RESTORATION MODULAR STEM CONSTRUCT WITH A CERAMIC HEAD AND NEW LINER. REP PROVIDED INTRA- OP PHOTOS AND AN EXPLANT PICTURE AND REPORTED THAT NO FURTHER INFORMATION WILL BE AVAILABLE.

  Patient problems: Injury

  MAUDE report 9295776 ↗
• InjuryOct 19, 2018Material Deformation; Material Deformation

  PATIENT CALLED STATING HE HAD A LEFT HIP IMPLANT ON (B)(6) 2005. PATIENT NOTED THAT 2 MONTHS AGO AS HE GOT UP FROM USING THE BATHROOM HE NOTICED PAIN. PATIENT STATED HIS PELVIS AND FEMUR DISCONNECTED. PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2018 TO STRYKER DEVICES.

  Patient problems: Injury; Joint Dislocation; Pain

  MAUDE report 7984813 ↗