Skip to content

Brasseler USA 5010175M0Recalls & reported problems

Peter Brasseler Holdings, LLC · K7-1990-50 90.0 X 19.0 MM · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887919526230), received between Apr 14, 2023 and Apr 14, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Use of Device Problem” (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

Device problems

  • Use of Device Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionApr 14, 2023Use of Device Problem; Use of Device Problem

    THE CUSTOMER REPORTED THAT A LARGE BONE BLADE BROKE WHILE MAKING FEMORAL CUTS IN A TOTAL KNEE PROCEDURE WHILE MAKING THE FEMUR CUT. THE PATIENT WAS NOT INJURED. MEDWATCH FORM 5115967 WAS RECEIVED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16742222 ↗

Other BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL devices

All BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page