Trident 69-2244Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327025446), received between Apr 25, 2019 and Sep 25, 2026 — classified as 3 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjurySep 25, 2026Device Dislodged or Dislocated

  Patient problems: Joint Dislocation

  MAUDE report 50896021 ↗
• InjuryJun 13, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  SURGEON REPORTED THAT THE PATIENT HAS UNDERGONE AN URGENT REVISION RIGHT TOTAL HIP REPLACEMENT DUE TO DISLOCATION OF CONSTRAINED LINER. ACETABULUM: 44MM STRYKER TRIDENT CONSTRAINED LINER WAS STILL ENGAGED WITH THE HEAD AND THEREFORE DISENGAGED WITH THE REMOVAL KEY. STRYKER REP REPORTED THAT THE BIPOLAR HEAD CAN BE RETURNED, THE OUTER BEARING HAD TO BE REAMED AND THEREFORE NOT AVAILABLE FOR RETURN. FEMUR: CHARNLEY STEM MOVED AND CEMENT MENTAL RETAINED. SURGEON INSPECTED THE STEM AND DECLARED NO EVIDENCE OF WEAR OR IMPINGEMENT. DISLOCATION OCCURRED ON 13TH MAY AND SURGEON EXPLAINED THAT PATIENT WAS SAT WASHING HIS FOOT WITH THE RIGHT LEG IN A FIGURE OF 4 POSITION.

  Patient problems: Injury

  MAUDE report 8695412 ↗
• InjuryApr 25, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED. AS REPORTED BY REP: "PATIENT DISLOCATED, DISASSOCIATING THE [COMPETITOR] INNER BIPOLAR COMPONENT FROM THE CONSTRAINED LINER". A STRYKER 44MM ALL POLY CONSTRAINED LINER WAS SWAPPED FOR ANOTHER 44MM ALL POLY CONSTRAINED LINER. REP REPORTED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Injury

  MAUDE report 8552067 ↗