EZX Blade BRXTB530Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887919859130), received between Mar 19, 2026 and Mar 19, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 19, 2026Break

  LEFT TOTAL HIP REVISION, BRASSELER EZX BLADE OPENED TO STERILE FIELD. WHILE SURGEON USING INSIDE LEFT HIP BLADE BROKE. ALL PIECES RETRIEVED FROM LEFT HIP. C-ARM WAS OFFERED, BUT SURGEON DETERMINED ALL PIECES RETRIEVED AND NO NEED FOR IMAGING.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24636771 ↗