CAPRI™ Corpectomy Cage System 2112-90007Recalls & reported problems

Summary

The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 10888857033641), received between Oct 29, 2020 and Feb 26, 2026 — classified as 12 malfunctions.

The most frequently reported specific device problem is “Material Deformation” (12 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

Recent adverse event reports

The 12 most recent of 12 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 24464432 ↗
• MalfunctionFeb 26, 2026Material Deformation

  NO NEW INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24464431 ↗
• MalfunctionApr 14, 2022Material Deformation; Material Deformation

  IT WAS REPORTED THAT OUTSIDE THE OR THE TIPS OF TWO CAPRI HEIGHT EXPANSION DRIVERS LOOKED WORN. THE REPORTED EVENT WAS NOTED DURING INSPECTION. THERE IS NO PROCEDURE ASSOCIATED WITH THIS REPORTED EVENT, NO PATIENT INVOLVEMENT, AND NO ADVERSE CONSEQUENCE HAS BEEN REPORTED. THIS REPORT CAPTURES THE SECOND HEIGHT EXPANSION DRIVER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14116265 ↗
• MalfunctionApr 14, 2022Material Deformation; Material Deformation

  IT WAS REPORTED THAT OUTSIDE THE OR THE TIPS OF TWO CAPRI HEIGHT EXPANSION DRIVERS LOOKED WORN. THE REPORTED EVENT WAS NOTED DURING INSPECTION. THERE IS NO PROCEDURE ASSOCIATED WITH THIS REPORTED EVENT, NO PATIENT INVOLVEMENT, AND NO ADVERSE CONSEQUENCE HAS BEEN REPORTED. THIS REPORT CAPTURES THE FIRST HEIGHT EXPANSION DRIVER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14116210 ↗
• 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 SECOND HEIGHT EXPANSION DRIVER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14115790 ↗
• 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 FIRST HEIGHT EXPANSION DRIVER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14115763 ↗
• MalfunctionDec 13, 2021Material Deformation; Material Deformation

  IT WAS REPORTED THAT A CAPRI EXPANDABLE HEIGHT EXPANSION DRIVER "NO LONGER GRIPS THE SCREW HEAD" AFTER CLEANING/STERILIZATION. THERE IS NO PROCEDURE ASSOCIATED WITH THIS REPORTED EVENT, NO PATIENT INVOLVEMENT, AND NO ADVERSE CONSEQUENCE HAS BEEN REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12987746 ↗
• 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 HEIGHT EXPANSION DRIVERS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12740818 ↗
• 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 HEIGHT EXPANSION DRIVERS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12737633 ↗
• MalfunctionApr 2, 2021Material Deformation; Insufficient Device Problem Information; Material Deformation; Insufficient Device Problem Information

  A COMPANY REPRESENTATIVE REPORTED TWO CAPRI HEIGHT EXPANSION DRIVERS CHANGED THE LORDOSIS OF A CAPRI EXPANDABLE CAGE RATHER THAN THE HEIGHT (AS THE PHYSICIAN INTENDED). AFTER SEEING THE CHANGE IN LORDOSIS IN THE X-RAY, THE PHYSICIAN ATTEMPTED TO DECREASE THE HEIGHT OF THE CAGE BUT WAS UNABLE TO, REPORTING THAT THE CAGE HAD "STRIPPED." THE PHYSICIAN COMPLETED THE CASE WITH A 30-MINUTE DELAY AND REPORTED THAT, "THE DISTRACTION FIT WAS ACCEPTABLE TO FINISH THE CASE BUT NOT IDEAL FOR THE PATIENT." THIS REPORT CAPTURES THE SECOND OF TWO CAPRI HEIGHT EXPANSION DRIVERS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11608919 ↗
• MalfunctionApr 2, 2021Material Deformation; Insufficient Device Problem Information; Material Deformation; Insufficient Device Problem Information

  A COMPANY REPRESENTATIVE REPORTED TWO CAPRI HEIGHT EXPANSION DRIVERS CHANGED THE LORDOSIS OF A CAPRI EXPANDABLE CAGE RATHER THAN THE HEIGHT (AS THE PHYSICIAN INTENDED). AFTER SEEING THE CHANGE IN LORDOSIS IN THE X-RAY, THE PHYSICIAN ATTEMPTED TO DECREASE THE HEIGHT OF THE CAGE BUT WAS UNABLE TO, REPORTING THAT THE CAGE HAD "STRIPPED." THE PHYSICIAN COMPLETED THE CASE WITH A 30-MINUTE DELAY AND REPORTED THAT, "THE DISTRACTION FIT WAS ACCEPTABLE TO FINISH THE CASE BUT NOT IDEAL FOR THE PATIENT." THIS REPORT CAPTURES THE FIRST OF TWO CAPRI HEIGHT EXPANSION DRIVERS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11608916 ↗
• MalfunctionOct 29, 2020Mechanical Problem; Material Deformation; Mechanical Problem; Material Deformation

  IT WAS REPORTED THAT THE CAPRI HEIGHT EXPANSION DRIVER NO LONGER "LOCKS SECURELY AND ADEQUATELY TO THE SCREW PLUG' INTRA-OPERATIVELY. SURGERY WAS SUCCESSFULLY COMPLETED WITH THE DEVICE AND A 10 MINUTE DELAY. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10759542 ↗