VBOSS 33660700Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327262681), received between Aug 22, 2017 and Feb 9, 2022 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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 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.

• InjuryFeb 9, 2022Mechanical Problem; Mechanical Problem

  IT WAS REPORTED THAT THE TIP OF A VBOSS SMALL CAGE INSERTER WAS LOOSE AND DISLODGED DURING CAGE INSERTION. SUBSEQUENTLY, IT MADE CONTACT WITH THE SPINAL CORD RESULTING IN A DECREASE IN MEP VALUES. MEP VALUES RECOVERED AND SURGERY WAS SUCCESSFULLY COMPLETED.

  Patient problems: Spinal Column Injury

  MAUDE report 13499334 ↗
• MalfunctionAug 22, 2017Material Deformation; Mechanical Jam; Device Operates Differently Than Expected; Material Deformation; Mechanical Jam

  IT WAS REPORTED THAT; DURING SURGERY, THE INSERTER WAS NOT FUNCTIONAL. THE INNER SHAFT WAS NOT LINKED TO THE DIAL. AFTER THAT, THE SURGEON INSERTED THE CAGE WITH A FORCEPS.

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

  MAUDE report 6811849 ↗