GLOBAL CAP 2230-82-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295105121), received between Mar 22, 2018 and Apr 3, 2023 — classified as 3 malfunctions.

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

• MalfunctionApr 3, 2023Break; Device-Device Incompatibility; Break; Device-Device Incompatibility

  IT WAS REPORTED THAT THE STOP ON THE CRUCIFORM PUNCH WILL NOT LOCK ONTO THE HANDLE. NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16665276 ↗
• MalfunctionDec 22, 2021Break; Break

  ADDITIONAL INFORMATION RECEIVED INDICATED THAT THE INSTRUMENT DID NOT BREAK INTO TWO PIECES. THE SLEEVE, WHICH WAS ATTACHED TO THE PUNCH, DETACHED.

  Patient problems: Insufficient Information

  MAUDE report 13063818 ↗
• MalfunctionMar 22, 2018Break; Break

  IT WAS REPORTED THAT THE LOCKING TAB IS BROKEN AND THE INSTRUMENT WILL NOT LOCK INTO A FIXED POSITION. NO SURGICAL DELAY. ALL PIECES WERE RETRIEVED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7361246 ↗