EVEREST® Spinal System 2901-B60500Recalls & reported problems
VB Spine LLC · 2901-B60500 · Class 2 · Implant
- 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 10888857040939), received between Nov 11, 2025 and Nov 11, 2025 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 11, 2025Fracture; Fracture
A COMPANY REPRESENTATIVE REPORTED THAT AN EVEREST ROD FRACTURED POST-OPERATIVELY. ADDITIONAL DETAIL IS NOT AVAILABLE AT THIS TIME.
Patient problems: Insufficient Information
MAUDE report 23528864 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.