CAPRI™ Corpectomy Cage System 7501-90025Recalls & reported problems
VB Spine LLC · Driver Height/Angle · Class 2
All models of CAPRI Corpectomy Cage System (20)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 10888857361911), received between Mar 24, 2022 and Jun 29, 2026 — classified as 12 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (11 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
- Material Deformation11
- Mechanical Jam1
- No Apparent Adverse Event1
Patient problems
- No Clinical Signs, Symptoms or Conditions12
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 29, 2026Material Deformation
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CAPRI HEIGHT/ANGLE DRIVERS WERE OBSERVED TO BE DEFORMED AFTER A PROCEDURE DURING PROCESSING. THE ASSOCIATED PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT CAPTURES THE SECOND OF TWO DRIVERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25661339 ↗MalfunctionJun 29, 2026Material Deformation
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CAPRI HEIGHT/ANGLE DRIVERS WERE OBSERVED TO BE DEFORMED AFTER A PROCEDURE DURING PROCESSING. THE ASSOCIATED PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT CAPTURES THE FIRST OF TWO DRIVERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25661315 ↗MalfunctionMar 9, 2026Material Deformation
Component Description (g),Component Code FDA (g),Component Code IMDRF (g);Tip,3123,G04129;
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24550783 ↗MalfunctionMar 9, 2026Material Deformation; No Apparent Adverse Event
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CAPRI HEIGHT EXPANSION DRIVERS DEFORMED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT CAPTURES THE FIRST OF TWO HEIGHT EXPANSION DRIVERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24550769 ↗MalfunctionJan 12, 2026Material Deformation
A COMPANY REPRESENTATIVE REPORTED THAT THE TIP OF A CAPRI HEIGHT/ANGLE DRIVER DEFORMED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A FIVE MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24046489 ↗MalfunctionOct 3, 2025Material Deformation; Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23213158 ↗MalfunctionSep 4, 2025Material Deformation; Material Deformation
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CAPRI SMALL EXPANDABLE HEIGHT/ANGLE DRIVERS HAVE BECOME DEFORMED AND WERE NOT ADEQUATELY ENGAGING WITH SCREWS INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT CAPTURES THE SECOND OF TWO CAPRI SMALL EXPANDABLE HEIGHT/ANGLE DRIVERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22970522 ↗MalfunctionSep 4, 2025Material Deformation; Material Deformation
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CAPRI SMALL EXPANDABLE HEIGHT/ANGLE DRIVERS HAVE BECOME DEFORMED AND WERE NOT ADEQUATELY ENGAGING WITH SCREWS INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT CAPTURES THE FIRST OF TWO CAPRI SMALL EXPANDABLE HEIGHT/ANGLE DRIVERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22970517 ↗MalfunctionJun 17, 2025Material Deformation; Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22244545 ↗MalfunctionJul 7, 2022Mechanical Jam; Mechanical Jam
A COMPANY REPRESENTATIVE REPORTED THAT A CAPRI SMALL EXPANDABLE HEIGHT/ANGLE DRIVER JAMMED DURING INTRA-OPERATIVE EXPANSION OF A CAGE. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14949115 ↗MalfunctionMar 24, 2022Material Deformation; Material Deformation
IT WAS REPORTED THAT THE TIPS OF 2 CAPRI SMALL EXPANDABLE DRIVERS WERE BENT INTRA-OPERATIVELY. SURGERY WAS SUCCESSFULLY COMPLETED WITH A REPLACEMENT DRIVER AND NO DELAY. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED. THIS REPORT WILL CAPTURE THE SECOND OF TWO DRIVERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13895785 ↗MalfunctionMar 24, 2022Material Deformation; Material Deformation
IT WAS REPORTED THAT THE TIPS OF 2 CAPRI SMALL EXPANDABLE DRIVERS WERE BENT INTRA-OPERATIVELY. SURGERY WAS SUCCESSFULLY COMPLETED WITH A REPLACEMENT DRIVER AND NO DELAY. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED. THIS REPORT WILL CAPTURE THE FIRST OF TWO DRIVERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13895349 ↗
Other Spinal vertebral body replacement device devices
- GIZA Corpectomy implant Giza, Diam 14 mm, 23-32 mm, 7-10 DegEden Spine Europe SA · Spinal Vertebral Body Replacement Device1 recall0 reports
- X-CORE 7160012Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7220018Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7160014Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7180018Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7180016Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- GIZA Corpectomy implant Giza, Diam 14 mm, 18-22 mm, 2-5 DegEden Spine Europe SA · Spinal Vertebral Body Replacement Device1 recall0 reports
- GIZA Corpectomy implant Giza, Diam 14 mm, 23-32 mm, 2-5 DegEden Spine Europe SA · Spinal Vertebral Body Replacement Device1 recall0 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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