CAPRI™ Corpectomy Cage System 2112-90009Recalls & reported problems
VB Spine LLC · Inserter Threaded Shaft · Class 2
All models of CAPRI Corpectomy Cage System (20)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10888857033665), received between Nov 6, 2020 and Feb 26, 2026 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (7 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 Deformation7
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 26, 2026Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24464438 ↗MalfunctionFeb 12, 2025Material Deformation; Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21368265 ↗MalfunctionFeb 12, 2025Material Deformation; Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21368262 ↗MalfunctionOct 28, 2022Material Deformation; Material Deformation
THIS RECORD IS A CONSOLIDATION OF Q3 2022 RECORDS SUMMARIZED AS A PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. THIS REPORT CAPTURES TWO INSTANCE OF INTRAOPERATIVE CAPRI LARGE EXPANDABLE INSERTER INNER SHAFT DEFORMATION. THE ASSOCIATED PROCEDURES WERE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO A PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15691994 ↗MalfunctionJun 22, 2022Material Deformation; Material Deformation
A COMPANY REPRESENTATIVE REPORTED THAT A CAPRI INSERTER, CAPRI INSERTER INNER SHAFT, AND CAPRI NON-TAPERED DRIVER WERE DAMAGED DURING SURGERY. THE SURGEON MALLETED THE INSERTER INTO THE PATIENT WHICH CAUSED DEFORMATION ON THE PROXIMAL END OF THE CAPRI INSERTER (MALLET MARKS) AND DEFORMATION ON THE DISTAL END OF THE CAPRI INSERTER INNER SHAFT. IMAGES PROVIDED INDICATE THE DISTAL END OF THE CAPRI NON-TAPERED DRIVER IS ALSO DEFORMED. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS RECORD CAPTURES THE CAPRI INSERTER INNER SHAFT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14780540 ↗MalfunctionMar 15, 2022Material Deformation; Material Deformation
IT WAS REPORTED THAT THE CAPRI INSERTER THREADED SHAFT WOULD NOT HOLD THE CAGE. SURGERY WAS SUCCESSFULLY COMPLETED WITH ANOTHER INSERTER AND NO DELAY. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13769796 ↗MalfunctionNov 6, 2020Fracture; Material Deformation; Fracture; Material Deformation
IT WAS REPORTED THAT A CAPRI INSERTER THREADED SHAFT BECAME DEFORMED INTRA-OPERATIVELY. THE SURGEON HIT THE DEVICE SEVERAL TIMES WITH A METAL MALLET DURING CAGE INSERTION AND COULD NOT REMOVE THE DRIVER. THE DEVICE WAS REMOVED BY HAMMERING THE T-HANDLE INTO THE SHAFT. SURGERY WAS SUCCESSFULLY COMPLETED WITH A 10 MINUTE DELAY. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10804584 ↗
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- 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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