CHS 71134052Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 03596010176400), received between Sep 28, 2021 and Apr 4, 2022 — 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 16, 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 4, 2022Break; Break

  IT WAS REPORTED THAT AN INTERMEDIATE BARREL GUIDE IS SPLIT/CRUSHED. AS THIS WAS NOTICED UPON FIELD INSPECTION, THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14002924 ↗
• MalfunctionFeb 14, 2022Break; Break

  IT WAS REPORTED THAT, AN INTERMEDIATE BARREL GUIDE BROKE. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13529731 ↗
• MalfunctionSep 28, 2021Break; Break

  IT WAS REPORTED THAT, DURING A HIP SCREW PROCEDURE, ONE INTERMEDIATE BARREL GUIDE BROKE. NO PIECES FELL INTO PATIENT. NO HARM TO PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12543952 ↗