EVEREST Spinal System 5101-90219Recalls & reported problems
VB Spine LLC · XT Support Tower Reducer · Class 1
All models of EVEREST Spinal System (77)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10888857325975), received between Sep 9, 2020 and Mar 21, 2023 — classified as 1 injury, 4 malfunctions.
The most frequently reported specific device problem is “Mechanical Jam” (5 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 16, 2026.
Most reported problems
Device problems
- Mechanical Jam5
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Bone Fracture(s)1
- Injury1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 21, 2023Mechanical Jam; Mechanical Jam
A COMPANY REPRESENTATIVE REPORTED THAT DURING A SCOLIOSIS CORRECTION CASE AN EVEREST XT SUPPORT TOWER AND AN EVEREST XT SUPPORT TOWER REDUCER JAMMED / BECAME STUCK TOGETHER. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 10 MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT IS FOR THE EVEREST XT SUPPORT TOWER REDUCER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16587162 ↗MalfunctionMar 2, 2023Mechanical Jam; Mechanical Jam
A COMPANY REPRESENTATIVE REPORTED THAT DURING A SCOLIOSIS CORRECTION CASE, AN EVEREST XT SUPPORT TOWER JAMMED AND BECAME STUCK IN AN EVEREST XT SUPPORT TOWER REDUCER. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 10 MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT IS FOR THE EVEREST XT SUPPORT TOWER REDUCER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16469095 ↗MalfunctionFeb 24, 2023Mechanical Jam; Mechanical Jam
A COMPANY REPRESENTATIVE REPORTED THAT DURING A SCOLIOSIS CORRECTION CASE TWO EVEREST XT SUPPORT TOWERS JAMMED / GOT STUCK IN TWO EVEREST XT SUPPORT TOWER REDUCERS. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 15 MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT IS FOR THE SECOND OF TWO EVEREST XT SUPPORT TOWER REDUCERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16437629 ↗MalfunctionFeb 24, 2023Mechanical Jam; Mechanical Jam
A COMPANY REPRESENTATIVE REPORTED THAT DURING A SCOLIOSIS CORRECTION CASE TWO EVEREST XT SUPPORT TOWERS JAMMED / GOT STUCK IN TWO EVEREST XT SUPPORT TOWER REDUCERS. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 15 MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT IS FOR THE FIRST OF TWO EVEREST XT SUPPORT TOWER REDUCERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16437622 ↗InjurySep 9, 2020Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT DURING INTRA-OPERATIVE ROD REDUCTION A SCREW BECAME STUCK IN AN EVEREST XT SUPPORT TOWER REDUCER AND THE REDUCER KNOB JAMMED CAUSING THE PEDICLE AT L5 TO BREAK. THE SURGEON WAS THEN UNABLE TO PLACE A SCREW AT THE RIGHT L5 LEADING TO ONLY UNILATERAL POSTERIOR FIXATION BEING ACHIEVED. THIS SUBSEQUENTLY LED TO AN APPROXIMATE 2-3 HOUR SURGICAL DELAY. THIS RECORD REPRESENTS THE XT SUPPORT TOWER REDUCER.
Patient problems: Bone Fracture(s); Injury
MAUDE report 10509838 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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