AVS Anchor-C 48321074Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04546540679369), received between Mar 30, 2017 and May 8, 2018 — classified as 2 malfunctions.

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

• MalfunctionMay 8, 2018Detachment of Device or Device Component; Detachment of Device or Device Component; Device Operates Differently Than Expected; Positioning Problem

  IT WAS REPORTED THAT DURING SURGERY, AN X-RAY INDICATED THAT THE SCREW ADVANCED BEYOND THE IMPLANT. THE ENTIRE CONSTRUCT (2 SCREWS, 1 CAGE) WERE REMOVED AND REPLACED WITH A CAGE AND A PLATE. UPON REMOVAL THE CAGE CAME APART. ALL FRAGMENTS WERE RETRIEVED. THERE WAS A REPORTED 20 MINUTE SURGICAL DELAY. NO REPORTS OF ADVERSE CONSEQUENCES TO THE PATIENT.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 7493379 ↗
• MalfunctionMar 30, 2017Break; Fracture; Difficult to Remove; Detachment of Device or Device Component; Material Integrity Problem; Fracture; Material Integrity Problem

  IT WAS REPORTED THAT; SURGEON HAD DIFFICULTY REMOVING SCREWS FROM CAGE. UPDATE (B)(6) 2017 THE PLATE OF THE CAGE BROKE OFF. EVERYTHING WAS RETRIEVED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6445576 ↗