AVS Anchor-C Cervical Cage System 48328625ARRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327276848), received between Feb 9, 2016 and Feb 9, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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.

• MalfunctionFeb 9, 2016Fracture; Material Integrity Problem; Break; Detachment Of Device Component; Fracture; Material Integrity Problem

  IT WAS REPORTED THAT THE SURGEON ATTEMPTED TO REMOVE A SCREW FROM A CAGE THAT WAS IMPLANTED. HE USED A REMOVAL DRIVER THAT COMES IN THE SET BUT WAS UNABLE TO GET THE SCREWDRIVER TO CONNECT INTO THE SCREW WITH THE DRAW ROD. HE LEFT THE SCREW IN PLACE AND DID NOT ATTEMPT TO REMOVE IT AGAIN. HE THEN NOTICED THAT THE TIP OF THE DRAW ROD WAS BROKEN OFF AND HE SAID IT WAS STUCK IN THE SCREW. THE SURGEON WAS NOT WORRIED ABOUT IT COMING OUT AND CLOSED THE PATIENT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 5419795 ↗