EVEREST® Spinal System 2911-07540Recalls & reported problems
VB Spine LLC · Polyaxial Screw Size Ø7.5x40 mm · Class 2 · Implant
All models of EVEREST Spinal System (77)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10888857042674), received between Jun 8, 2022 and Dec 22, 2025 — classified as 4 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information2
- Positioning Problem2
- Adverse Event Without Identified Device or Use Problem1
- Fracture1
Patient problems
- Insufficient Information3
- Failure of Implant2
- Unspecified Infection1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryDec 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A HEALTH PROFESSIONAL REPORTED THAT A PATIENT WAS REVISED APPROXIMATELY TWO YEARS AND THREE MONTHS POST-OPERATIVELY TO ADDRESS AN INFECTION AT THE IMPLANT SITE OF TWO UNKNOWN CAGES, ONE EVEREST MI CANNULATED POLYAXIAL SCREW AND ONE EVEREST POLYAXIAL SCREW. THIS REPORT CAPTURES THE EVEREST POLYAXIAL SCREW.
Patient problems: Unspecified Infection
MAUDE report 23874125 ↗InjuryDec 18, 2025Fracture; Fracture
InjuryJun 8, 2022Positioning Problem; Insufficient Device Problem Information; Positioning Problem; Insufficient Device Problem Information
A PATIENT WAS REVISED APPROXIMATELY TWO WEEKS AFTER IMPLANTATION TO ADDRESS TWO EVEREST POLYAXIAL SCREWS AT S1 WHICH, "LOST THEIR FIXATION." THIS REPORT CAPTURES THE FIRST OF TWO SCREWS.
Patient problems: Failure of Implant; Insufficient Information
MAUDE report 14633226 ↗InjuryJun 8, 2022Positioning Problem; Insufficient Device Problem Information; Positioning Problem; Insufficient Device Problem Information
A PATIENT WAS REVISED APPROXIMATELY TWO WEEKS AFTER IMPLANTATION TO ADDRESS TWO EVEREST POLYAXIAL SCREWS AT S1 WHICH, "LOST THEIR FIXATION." THIS REPORT CAPTURES THE SECOND OF TWO SCREWS.
Patient problems: Failure of Implant; Insufficient Information
MAUDE report 14633140 ↗
Other APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices
- EXPEDIUM 179702000Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL439 reports
- EXPEDIUM VERSE 199721001Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL227 reports
- XIA 3 48230000Stryker Corporation · APPLIANCE, FIXATION, SPINAL INTERLAMINAL193 reports
- VIPER 186715000Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 death167 reports
- NA 04.614.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL80 reports
- NA 04.615.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- EXPEDIUM VIPER 196789480Depuy Spine, LLC · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- Arsenal Deformity Spinal Fixation System 47127Alphatec Spine, Inc. · APPLIANCE, FIXATION, SPINAL INTERLAMINAL66 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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