Avenir Complete™ 574203020Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024509276), received between Sep 11, 2026 and Sep 11, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Difficult to Advance” (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 18, 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.

• InjurySep 11, 2026Difficult to Advance

  It was reported that during a primary total hip arthroplasty, a size 2 coxa vara femoral stem became firmly engaged distally during insertion and remained proud by approximately 1 to 2 cm, resulting in an intraoperative revision.During femoral preparation, the canal was rasped to size 2 and trialed with a coxa vara configuration, which was deemed to provide an appropriate fit. Upon implantation, the stem could not be advanced further despite multiple attempts. Extraction instruments were not available in theatre, necessitating an extended trochanteric osteotomy to facilitate removal. There was a significant intraoperative delay while additional instrumentation was transported from another site. Following removal of the stem, reconstruction was completed using an alternative stem and cone body.The patient underwent an extended trochanteric osteotomy and was reconstructed intraoperatively with an alternative stem and cone body.Attempts have been made and no further information has been provided.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50725408 ↗