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EVEREST® Spinal System 2911-08555Recalls & reported problems

VB Spine LLC · 2911-08555 · Class 2 · Implant

All models of EVEREST Spinal System (77)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888857043091), received between May 20, 2020 and May 20, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

Device problems

  • Fracture1

Patient problems

  • Injury1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 20, 2020Fracture; Fracture

    IT WAS REPORTED THAT AN EVEREST LOCKING SCREW INSERTER JAMMED AND AN EVEREST POLYAXIAL SCREW FRACTURED INTRA-OPERATIVELY. WHEN THE SURGEON ATTEMPTED TO REMOVE THE SCREW, THE SCREW HEAD POPPED OFF AND WAS STUCK ON THE INSTRUMENT. THERE WAS NO SURGICAL DELAY, HOWEVER THE PROCEDURE WAS NOT COMPLETED SUCCESSFULLY AS THE ROD WAS NOT ABLE TO BE CONNECTED AT THE DESIRED LEVEL AND THE SCREW SHAFT REMAINED IN THE PATIENT. THIS REPORT REPRESENTS THE SCREW.

    Patient problems: Injury; No Consequences Or Impact To Patient

    MAUDE report 10075403 ↗

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Sources and updates

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