Trident 69-2850Recalls & reported problems

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 07613327025477), received between Jul 3, 2018 and May 27, 2026 — classified as 11 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (9 reports).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Jul 30, 2026Open, Classified

   Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.

   Z-3201-2026 · Root cause: Process change control · FDA record ↗

Most reported problems

Recent adverse event reports

The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.

• InjuryMay 27, 2026Adverse Event Without Identified Device or Use Problem

  THE FOLLOWING INFORMATION WAS PROVIDED: PT. PRESENTED WITH AN INFECTION OF THE RIGHT-HIP FOLLOWING IMPLANTATION OF A CEMENTED TRIDENT ALL-POLY LINER AND COMPETITOR TOTAL-FEMUR CONSTRUCT. DR. OPTED TO PERFORM AN EXTENSIVE I&D AND REVISE TO AN ANTIBIOTIC SPACER OF SORTS. THE EXPLANTED TRIDENT ALL-POLY WAS REVISED WITH THE SAME SIZE LINER FOR THIS SURGERY. SCREWS WERE USED AS "REBAR, TO HELP GIVE THE LINER MORE SUPPORT WITHIN THE CEMENT-MANTLE BENEATH/BEHIND IT." NO COMPLAINTS WERE FILED AGAINST THE COMPONENTS THEMSELVES, NO FURTHER INFO AVAILABLE.

  Patient problems: Unspecified Infection

  MAUDE report 25305677 ↗
• InjuryJan 8, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THE FOLLOWING WAS REPORTED: "THE BIPOLAR LINER IN THE CEMENTED ALL POLY CONSTRAINT CUP DISLOCATED. REVISION SURGERY HAD TO BE PERFORMED."

  Patient problems: Ambulation or Postural Difficulties

  MAUDE report 21102577 ↗
• InjuryNov 7, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  AS REPORTED: "REV RTHA. SHE IS CHRONIC DISLOCATOR AND THE DOCTOR DECIDED TO GO WITH A COMPETITOR." REP CONFIRMED THE INNER BIPOLAR HEAD OF THE CONSTRAINED INSERT DISSOCIATED FROM THE OUTER POLY. REP ALSO CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Joint Dislocation

  MAUDE report 20628527 ↗
• InjuryFeb 13, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT HAS BEEN REPORTED THAT THERE WAS A TRIDENT CEMENTED CONSTRAINED LINER IMPLANTED DURING A REVISION SURGERY. AFTER THE REDUCTION OF THE HIP, THE INNER PART OF THE CONSTRAINED LINER + THE FEMORAL HEAD DISASSOCIATED FROM THE EXTERNAL PART OF THE LINER, WHICH STAYED IN THE PATIENT (SINCE IT WAS CEMENTED IN THE SOCKET). IT WAS IMPOSSIBLE TO PERFORM THE REDUCTION AGAIN, SO THE SURGEON PROCEED TO EXTRACT THE LINER, WHICH CAME OUT TOGETHER WITH THE CEMENT MANTLE AND THE ANTERIOR WALL OF THE ACETABULUM OF THE PATIENT.

  Patient problems: Injury

  MAUDE report 9708838 ↗
• InjuryOct 14, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  DISLOCATION OF TRIDENT ALL-POLY CEMENTED CUP.

  Patient problems: Injury; Joint Dislocation

  MAUDE report 9186297 ↗
• InjuryAug 21, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THIS PATIENT DISLOCATED AGAIN ON THE WARD ON THE 22ND. AGAIN THE CONSTRAINED ACETABULAR LINER APPEARED DISASSOCIATED ON X-RAY. A REVISION HIP WAS PERFORMED TODAY (THE LAST REVISION PERFORMED BY A (PREVIOUS DOCTOR AND HE IS ON ANNUAL LEAVE). THE DEVICE WAS REASSEMBLED (PUSHING THE LARGE BALL PAST THE RETAINING RING TO RELOCATE INTO THE LINER). A FORM OF DACRON SLING WAS USED TO PREVENT END OF RANGE IMPINGEMENT OF THE HIP STEM NECK ON THE CONSTRAINED LINER. THE DR. HAS ALLOWED PLAIN X-RAYS AND INTRO- OPERATIVE PICTURES TO BE SENT BUT THE OPERATIVE NOTES ARE NOT AVAILABLE.

  Patient problems: Injury

  MAUDE report 8917326 ↗
• InjuryJul 30, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  DISLOCATION LEFT PROSTHETIC HIP REPLACEMENT. CONSTRAINED CEMENTED LINER IN SITU. REVISION HIP SURGERY (B)(6). APPARENT DISLOCATION AND DISSOCIATION OF STRYKER CEMENTED CONSTRAINED LINER (LARGE ARTICULATING HEAD WITH OUTER CASING). LINER WAS REVISED WITH A NEW DEVICE OF THE SAME CATEGORY NUMBER. THE FEMORAL STEM WAS REVISED FOR ACETABULAR ACCESS. PRIMARY HIP SURGERY APPROXIMATELY 4 WEEKS AGO. CUSTOM HEMIPELVIC TUMOUR PROSTHESIS WITH STRYKER ALL POLY CONSTRAINED LINER 50MM, EXETER 44 NO 0 HIP STEM AND 28 + 0 HEAD. THE EXACT ITEM AND LOT CODES ARE NOT YET AVAILABLE.

  Patient problems: Injury; Joint Dislocation

  MAUDE report 8841778 ↗
• InjuryApr 23, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED. AS REPORTED: "PRE-OP DIAGNOSIS: RIGHT FAILED HIP. SURGEON COMMENTS: STEM IS LOOSE, THIGH PAIN. PRE-OP NOTES: PATIENT HAS INCREASED PAIN, INCREASED DISABILITY WITH AMBULATION". A COMPETITOR STEM AND HEAD, AND A STRYKER LINER WERE REVISED. REP PROVIDED A PRE-REVISION X-RAY AND REPORTED THAT NO FURTHER INFORMATION WILL BE AVAILABLE.

  Patient problems: Injury; Pain

  MAUDE report 8540664 ↗
• InjuryApr 17, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT CAME TO DOCTOR AND COMPLAIN ABOUT FEELING PAIN WHILE WALKING, AFTER X-RAY FOUND THAT TRIDENT V40 HEAD DISLOCATION.

  Patient problems: Injury; Pain

  MAUDE report 8522651 ↗
• InjuryJul 3, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THE PATIENT HAD REVISION SURGERY ON (B)(6) 2018. IT WAS REPORTED THAT THE IMPLANT FAILED WHILE THE PATIENT LAY IN BED AND TURNED OVER. THE REP CONFIRMED THAT THE PATIENT¿S TOTAL FEMUR WAS EXTENDED BY 15MM. THIS INDICATED THAT THERE COULD HAVE BEEN SOFT TISSUE LAXITY/STRETCHING. THE REP UNDERSTANDS THAT THE INNER HEAD AND LOCKING RING DISLOCATED FROM THE CUP BODY.

  Patient problems: Injury; Joint Dislocation

  MAUDE report 7659712 ↗
• InjuryJul 3, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THE PATIENT HAD SURGERY. THE REP UNDERSTANDS THAT THE INNER HEAD AND LOCKING RING HAS DISLOCATED FROM THE CUP BODY. THE PATIENT HAD A REVISION.

  Patient problems: Injury; Joint Dislocation

  MAUDE report 7659393 ↗