CAPRI™ Corpectomy Cage System 2112-90005Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10888857033627), received between Oct 19, 2020 and Apr 19, 2022 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Fracture” (2 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 19, 2022Material Separation; Material Separation

  A COMPANY REPRESENTATIVE REPORTED THAT A CAPRI ANTI-TORQUE HANDLE, "FELL APART DURING SURGERY." 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 14147748 ↗
• MalfunctionJan 4, 2021Fracture; Fracture

  IT WAS REPORTED THAT THE CAPRI LARGE EXPANDABLE ANTI TORQUE HANDLE FRACTURED INTRA-OPERATIVELY. THE FRACTURED PIECES WERE REMOVED FROM THE SURGICAL SITE AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 5 MINUTE DELAY. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11112107 ↗
• MalfunctionOct 19, 2020Fracture; Fracture

  IT WAS DISCOVERED THAT A CAPRI LARGE EXPANDABLE ANTI TORQUE HANDLE "BROKE INTO 3 PARTS" AFTER THE PROCEDURE WAS COMPLETED SUCCESSFULLY. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT OR SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10701980 ↗