CAPRI Corpectomy Cage SystemRecalls & reported problems across all models
VB Spine LLC · 20 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 58
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls
- 0
We found 20 models of CAPRI Corpectomy Cage System by VB Spine LLC in the FDA's device registry (GUDID). Together they are named in 58 adverse event reports in the FDA's MAUDE database, received between Oct 19, 2020 and Jun 29, 2026 — classified as 4 injuries, 54 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (42 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported CAPRI Corpectomy Cage System problems
Device problems
- Material Deformation42
- Fracture10
- Mechanical Jam6
- Mechanical Problem5
- Material Twisted/Bent4
- Insufficient Device Problem Information3
- Migration2
- Device Dislodged or Dislocated1
Patient problems
- No Clinical Signs, Symptoms or Conditions55
- Pain3
CAPRI Corpectomy Cage System models
20 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CAPRI™ Corpectomy Cage System 2112-90007SPINAL VERTEBRAL BODY REPLACEMENT DEVICE12 reports
- CAPRI™ Corpectomy Cage System 7501-90025Spinal vertebral body replacement device12 reports
- CAPRI™ Corpectomy Cage System 2112-90009SPINAL VERTEBRAL BODY REPLACEMENT DEVICE7 reports
- CAPRI™ Corpectomy Cage System 2112-90006SPINAL VERTEBRAL BODY REPLACEMENT DEVICE4 reports
- CAPRI Corpectomy Cage System 2112-90020Orthopedic manual surgical instrument4 reports
- CAPRI™ Corpectomy Cage System 2112-90005ORTHOPEDIC MANUAL SURGICAL INSTRUMENT3 reports
- CAPRI™ Corpectomy Cage System 2112-90008SPINAL VERTEBRAL BODY REPLACEMENT DEVICE3 reports
- CAPRI Corpectomy Cage System 2112-20830SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 report
- CAPRI Corpectomy Cage System 2112-20836SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 report
- CAPRI Corpectomy Cage System 2112-21625SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 report
- CAPRI Corpectomy Cage System 2112-90019Orthopedic manual surgical instrument1 report
- CAPRI™ Corpectomy Cage System 2112-90053SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 report
- CAPRI™ Corpectomy Cage System 7512-21628L0-G3Spinal vertebral body replacement device1 report
- CAPRI™ Corpectomy Cage System 7512-21846L0-G3Spinal vertebral body replacement device - Cervical1 report
- CAPRI™ Corpectomy Cage System 7512-21636L0-G3Spinal vertebral body replacement device - Cervical1 report
- CAPRI™ Corpectomy Cage System 7512-21621L0-G3Spinal vertebral body replacement device1 report
- CAPRI™ Corpectomy Cage System 7512-21624L0-G3Spinal vertebral body replacement device - Cervical1 report
- CAPRI™ Corpectomy Cage System 7501-10001-G1Spinal vertebral body replacement device1 report
- CAPRI™ Corpectomy Cage System 7512-21421L0-G3Spinal vertebral body replacement device - Cervical1 report
- CAPRI™ Corpectomy Cage System 7512-21428L0-G3Spinal vertebral body replacement device1 report
Recent CAPRI Corpectomy Cage System adverse event reports
The 15 most recent reports across all models, 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 ↗MalfunctionJun 9, 2026Fracture; Material Deformation
A COMPANY REPRESENTATIVE REPORTED THAT THE TIP OF A CAPRI LORDOSIS/KYPHOSIS DRIVER INNER SHAFT DEFORMED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25448022 ↗InjuryMar 9, 2026Migration
MalfunctionMar 9, 2026Device Dislodged or Dislocated
A HEALTH PROFESSIONAL REPORTED THAT AN ENDPLATE PIN OF A CAPRI INTERNAL EXPANSION TOWER DISENGAGED INTRA-OPERATIVELY. THIS WAS OBSERVED IN AN INTRA-OPERATIVE X-RAY. THE SURGEON DECIDED TO LEAVE THE DEVICE IMPLANTED IN THE PATIENT. NO ADVERSE CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24552820 ↗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 ↗MalfunctionFeb 26, 2026Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24464438 ↗MalfunctionFeb 26, 2026Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24464432 ↗MalfunctionFeb 26, 2026Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24464431 ↗MalfunctionFeb 5, 2026Mechanical Jam
A COMPANY REPRESENTATIVE REPORTED THAT A CAPRI EXPANDABLE CORPECTOMY CAGE WITH SET SCREW WAS UNABLE TO EXPAND INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A FIVE-MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCES TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24273223 ↗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 ↗
Other VB Spine LLC products
- EVEREST Spinal System77 models · 336 reports · 3 recalls
- YUKON OCT Spinal System54 models · 238 reports · 3 recalls
- OZARK Cervical Plate System54 models · 270 reports
- MESA Spinal System55 models · 140 reports
- ALEUTIAN Interbody Systems37 models · 135 reports
- CHESAPEAKE Stabilization System31 models · 46 reports · 1 recall
- PYRENEES Cervical Plate System29 models · 96 reports
- DENALI Spinal System22 models · 80 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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