Avenir Complete™ 574201050Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024509047), received between Oct 15, 2020 and Dec 15, 2022 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Separation Failure” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryDec 15, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT AFTER THE PATIENT UNDERWENT A RIGHT TOTAL HIP REPLACEMENT, IT WAS FOUND THAT THE PATIENT HAD OSTEOPOROTIC BONE QUALITY AND SUSTAINED A NON-DISPLACED CALCAR FRACTURE DURING STEM IMPACTION. TWO 1.7MM CERCLAGE CABLES WERE PLACED INTRAOPERATIVELY. SURGERY COMPLETED WITHOUT FURTHER COMPLICATIONS. NO ADDITIONAL INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Bone Fracture(s); Osteopenia/ Osteoporosis

  MAUDE report 15985855 ↗
• MalfunctionOct 15, 2020Separation Failure; Separation Failure

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10682904 ↗