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CAPRI Corpectomy Cage System 2112-90019Recalls & reported problems

VB Spine LLC · Driver Size 20 · Class 1

All models of CAPRI Corpectomy Cage System (20)

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888857211582), received between Apr 14, 2022 and Apr 14, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Deformation” (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

  • Material Deformation1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionApr 14, 2022Material Deformation; Material Deformation

    IT WAS REPORTED THAT 2 CAPRI HEIGHT EXPANSION DRIVERS, 1 LORDOSIS/KYPHOSIS EXPANSION DRIVER, 1 NON-TAPERED DRIVER, AND 1 DRIVER WERE ALL STRIPPED AT THE TIP OUTSIDE THE OPERATING ROOM. THERE WAS NO ASSOCIATED PROCEDURE WITH THIS EVENT, THEREFORE, NO ADVERSE CONSEQUENCES TO ANY PATIENTS WERE SEEN. THIS REPORT CAPTURES THE DRIVER.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14115795 ↗

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Sources and updates

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