Avenir Complete™ 574101030Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024508637), received between Feb 10, 2022 and Feb 10, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 10, 2022Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING AN INITIAL HIP SURGERY THE SURGEON BROACHED TO A SIZE 3 AVENIR THEN PROCEEDED WITH A TRIAL REDUCTION, THE SIZE 3 STD AVENIR IMPLANT WAS THEN IMPACTED AND SAT 10MM PROUD FROM THE RESECTION LEVEL. AT THIS POINT, THE SURGEON DECIDED TO REMOVE THE IMPLANT TO CHECK TOLERANCES FOR RETURN. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13508799 ↗