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

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327267181), received between Aug 16, 2017 and Dec 26, 2018 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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 18, 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.

• MalfunctionDec 26, 2018Material Deformation; Break; Material Deformation

  IT WAS REPORTED THAT THE SCREW EXTRACTOR TIP WAS DAMAGED WHILE TRYING TO REMOVE A PIECE OF SCREWDRIVER THAT SHEARED OF IN THE SCREW. THE SURGEON REMOVED THE CAGE AND SCREWS BY DRILLING AROUND THE IMPLANT TO FREE UP THE SCREWS ENOUGH TO PULL CAGE OUT. A SURGICAL DELAY TIME HAS NOT BEEN SPECIFIED. THE ADDITIONAL INFORMATION RECEIVED FROM THE SALES REP CONFIRMED THAT THE ROD THREADS WERE DAMAGED AND RESULTED IN ABOUT AN HOUR SURGICAL DELAY WHILE TRYING TO REMOVE THE SCREW WITH SCREWDRIVER FRAGMENTS IN STILL. NO OTHER ADVERSE CONSEQUENCE TO THE PATIENT WAS REPORTED.

  Patient problems: Injury; No Code Available; No Consequences Or Impact To Patient

  MAUDE report 8196018 ↗
• MalfunctionAug 16, 2017Material Deformation; Bent; Break; Material Deformation

  IT WAS REPORTED THAT; THE SURGEON ATTEMPTED TO USE THE SCREW EXTRACTOR. THE TIP OF THE SCREW EXTRACTOR DRAW ROD BROKE/BENT.

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

  MAUDE report 6798948 ↗