CAPRI™ Corpectomy Cage System 2112-90008Recalls & reported problems
VB Spine LLC · Lordosis/Kyphosis Expansion, Driver · Class 2
All models of CAPRI Corpectomy Cage System (20)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10888857033658), received between Nov 2, 2021 and Apr 14, 2022 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (3 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.
Most reported problems
Device problems
- Material Deformation3
- Material Twisted/Bent2
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 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 OR. THERE WAS NO ASSOCIATED PROCEDURE WITH THIS EVENT, THEREFORE, NO ADVERSE CONSEQUENCES TO ANY PATIENTS WERE SEEN. THIS REPORT CAPTURES THE LORDOSIS/KYPHOSIS EXPANSION DRIVER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14115802 ↗MalfunctionNov 2, 2021Material Deformation; Material Twisted/Bent; Material Deformation; Material Twisted/Bent
IT WAS REPORTED THAT THE TEETH OF TWO CAPRI LARGE LORDOSIS/KYPHOSIS DRIVERS AND TWO CAPRI LARGE HEIGHT EXPANSION DRIVERS DID NOT GRIP ONTO THE CAPRI INTERBODY AS INTENDED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 10 MINUTE SURGICAL DELAY. NO ADVERSE CONSEQUENCES NOR MEDICAL INTERVENTION WERE REPORTED. THIS RECORD CAPTURES THE FIRST OF THE TWO REPORTED CAPRI LARGE LORDOSIS/KYPHOSIS DRIVERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12737629 ↗MalfunctionNov 2, 2021Material Deformation; Material Twisted/Bent; Material Deformation; Material Twisted/Bent
IT WAS REPORTED THAT THE TEETH OF TWO CAPRI LARGE LORDOSIS/KYPHOSIS DRIVERS AND TWO CAPRI LARGE HEIGHT EXPANSION DRIVERS DID NOT GRIP ONTO THE CAPRI INTERBODY AS INTENDED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 10 MINUTE SURGICAL DELAY. NO ADVERSE CONSEQUENCES NOR MEDICAL INTERVENTION WERE REPORTED. THIS RECORD CAPTURES THE SECOND OF THE TWO REPORTED CAPRI LARGE LORDOSIS/KYPHOSIS DRIVERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12737628 ↗
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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