CAPRI Corpectomy Cage System 2112-90020Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10888857033702), received between Dec 20, 2021 and Jun 22, 2022 — classified as 4 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

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• 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 NON-TAPERED DRIVER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14780542 ↗
• 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 NON-TAPERED DRIVER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14115814 ↗
• MalfunctionApr 11, 2022Material Deformation; Material Deformation

  IT WAS REPORTED THAT THE TIP OF A SHORT CAPRI NON-TAPERED DRIVER WAS OBSERVED TO BE STRIPPED OUTSIDE OF THE OPERATING THEATER. 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 14077380 ↗
• MalfunctionDec 20, 2021Fracture; Mechanical Jam; Fracture; Mechanical Jam

  IT WAS REPORTED THAT A CAGE WAS UNABLE TO BE RELEASED FROM A CAPRI LARGE EXPANDABLE INSERTER INTRA-OPERATIVELY. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 20 MINUTE SURGICAL DELAY BY USING AN ALTERNATIVE CAGE AND INSERTER. THIS RECORD CAPTURES THE INSERTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13048128 ↗