Longevity® 110031000Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024572584), received between Mar 30, 2023 and Jul 10, 2025 — classified as 4 injuries.

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

3 other recalls cover devices cleared under the same FDA submission (K190656); they may or may not involve this specific model.

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryJul 10, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT APPROXIMATELY THREE YEARS POST-IMPLANTATION, THE PATIENT UNDERWENT A LEFT HIP REVISION DUE TO THE BEARING DISASSOCIATING FROM THE HEAD. THE BEARING WAS FOUND STUCK IN THE PELVIS AND WAS UNABLE TO BE RETRIEVED DURING THE PROCEDURE. A NEW BEARING AND HEAD WERE IMPLANTED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Joint Dislocation

  MAUDE report 22470595 ↗
• InjuryMar 4, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT A PATIENT HAD AN INITIAL RIGHT TOTAL HIP ARTHROPLASTY FOLLOWED BY A REVISION 1 MONTH LATER DUE TO UNRESOLVED PAIN AND WEAKNESS. DURING THIS PROCEDURE THE CUP WAS RETAINED BUT WAS NOTED AS ¿A LITTLE UNDER ANTEVERTED.¿ SUBSEQUENTLY, THE PATIENT WAS REVISED A SECOND TIME APPROXIMATELY 1 MONTH LATER FOLLOWING A TWISTING INJURY CAUSING PAIN AND DISLOCATION. THE STEM WAS RETAINED, AND ALL OTHER IMPLANTS WERE REVISED WITHOUT COMPLICATION.

  Patient problems: Joint Dislocation; Pain

  MAUDE report 21515832 ↗
• InjuryDec 31, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THERE IS NO UPDATE TO THE PRIOR EVENT DESCRIPTION PROVIDED.

  Patient problems: Joint Dislocation

  MAUDE report 21048607 ↗
• InjuryMar 30, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.

  Patient problems: Failure of Implant; Joint Dislocation; Muscle/Tendon Damage

  MAUDE report 16643361 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K190656. One submission often covers many models, so check the product and lot details in each record.

• Z-0419-2026 · Sep 26, 2025 · Open, Classified
  Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 46 mm O.D., Size G, Bearing, Model/Catalog Number: 110031013; semi constrained hip prosthesis
• Z-0418-2026 · Sep 26, 2025 · Open, Classified
  Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 44 mm O.D., Size F, Bearing, Model/Catalog Number: 110031012; semi constrained hip prosthesis
• Z-0057-2021 · Aug 14, 2020 · Terminated
  Dual Mobility Vivacit-E Bearing, Model Number 110031009