Avenir Complete® 574777110Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00889024509825), received between Feb 21, 2023 and Aug 6, 2026 — classified as 1 injury, 6 malfunctions.

The most frequently reported specific device problem is “Fracture” (6 reports).

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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 6, 2026Fracture

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50164554 ↗
• MalfunctionJan 12, 2026Device-Device Incompatibility; Damaged Thread

  IT WAS REPORTED THAT DURING THE HIP PROCEDURE, THE EXTRACTOR ADAPTER THREADS WERE DAMAGED AND IT WOULD NOT CONNECT WITH THE STEM. THERE WAS A DELAY LESS THAN 30 MINUTES AND THE SURGEON WAS ABLE TO REMOVE THE STEM. THERE WAS NO KNOWN IMPACT OR CONSEQUENCES TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24038339 ↗
• MalfunctionNov 20, 2025Fracture; Fracture

  IT WAS REPORTED THAT DURING THE SURGERY, THE EXTRACTOR ADAPTER BROKE OFF INSIDE THE STEM DURING EXTRACTION. THERE WAS NO KNOWN IMPACT OR CONSEQUENCES TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23608232 ↗
• MalfunctionApr 30, 2025Fracture; Fracture

  IT WAS REPORTED THAT DURING SURGERY, THE EXTRACTOR ADAPTER BROKE. THE TIP OF THE EXTRACTOR REMAINED IN THE STEM, WHICH WAS ABLE TO BE REMOVED WITH A DELAY OF ABOUT 15 MINUTES. NO PARTS WERE RETAINED IN THE PATIENT. THERE WAS NO KNOWN IMPACT OR CONSEQUENCES TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21935949 ↗
• InjuryApr 21, 2025Fracture; Fracture

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

  Patient problems: Foreign Body In Patient

  MAUDE report 21876740 ↗
• MalfunctionNov 6, 2023Fracture; Fracture

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18072283 ↗
• MalfunctionFeb 21, 2023Fracture; Fracture

  IT WAS REPORTED THAT DURING A RIGHT HIP REVISION, THE SURGEON WAS ATTEMPTING TO REMOVE THE STEM WHEN THE CONNECTING BOLT FOR THE SLAP HAMMER SHEARED OFF. THE STEM WAS NOT ABLE TO BE REMOVED AND THE BROKEN PIECE OF THE INSTRUMENT REMAINED IN THE WOUND. THE SURGEON DECIDED TO LEAVE THE STEM IMPLANTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Foreign Body In Patient

  MAUDE report 16408426 ↗