Avenir Complete™ 574202065Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00889024509191), received between Jan 31, 2024 and Dec 11, 2025 — classified as 3 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Degraded” (1 report).

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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryDec 11, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT APPROXIMATELY THREE YEARS POST-HIP IMPLANTATION, THE PATIENT HAS DEVELOPED TROCHANTERIC BURSITIS REQUIRING PHYSICAL THERAPY AND MEDICATION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Bursitis; Pain

  MAUDE report 23785902 ↗
• InjuryOct 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.

  Patient problems: Fall; Periprosthetic fracture

  MAUDE report 23232627 ↗
• MalfunctionAug 11, 2025Degraded; Degraded

  IT WAS REPORTED THAT THE SNAP-ON HEAD TRIALS FOR THE AVENIR ARE LEAVING BEHIND PIECES ON THE FINAL STEM WHEN TRIALING. NO KNOWN IMPACT OR CONSEQUENCE TO THE PATIENT. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22769842 ↗
• InjuryDec 30, 2024Patient-Device Incompatibility; Adverse Event Without Identified Device or Use Problem; Patient-Device Incompatibility; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE APPROPRIATE IMPLANT WAS SELECTED FOR THE PATIENT. SUBSEQUENT TO IMPLANTATION, THE PATIENT EXPERIENCED A PERIPROSTHETIC FRACTURE IN THE ACETABULUM. IT IS NOT KNOWN WHAT CAUSED THE FRACTURE. THE PATIENT WAS REVISED AND A LARGER IMPLANT USED AS A RESULT OF THE FRACTURE THAT HAD OCCURRED FOR BETTER FIXATION. THE PATIENT IS REPORTED TO BE DOING WELL AFTER THE REVISION SURGERY. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Bone Fracture(s); Joint Laxity

  MAUDE report 21037160 ↗
• MalfunctionJan 31, 2024Positioning Failure; Difficult to Insert; Inadequacy of Device Shape and/or Size; Positioning Failure; Difficult to Insert; Inadequacy of Device Shape and/or Size

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18613183 ↗