HALL® 00507126700Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20845854045968), received between Jul 29, 2024 and Jul 29, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Fragmentation” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 29, 2024Material Fragmentation; Material Fragmentation

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE 00507126700, OSCILLATOR BLADE, COATED, 19.5 X 95 X 1.27 MM, 5PK WAS BEING USED ON (B)(6) 2024 DURING A KNEE REPLACEMENT AND ¿THE TOOTH OF AN OSCILLATING BLADE BROKE OFF AND FELL INTO THE PATIENT¿. THERE WAS NO IMPACT OR INJURY FOR THE PATIENT OR USER. THE PROCEDURE WAS COMPLETED WITH A ¿DIFFERENT BLADE¿. THERE WAS A 45 MINUTE DELAY USING C ARM TO FIND BLADE TOOTH. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19850807 ↗
• MalfunctionJul 29, 2024Material Fragmentation; Material Fragmentation

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE 00507126700, OSCILLATOR BLADE, COATED, 19.5 X 95 X 1.27 MM, 5PK WAS BEING USED DURING A TOTAL HIP ARTHROPLASTY AND ¿THE TOOTH OF AN OSCILLATING BLADE BROKE OFF AND FELL INTO THE PATIENT DURING A THA. DELAY OF 40 MINUTES.¿ THERE WAS NO IMPACT OR INJURY FOR THE PATIENT OR USER. THE PROCEDURE WAS COMPLETED WITH A ¿DIFFERENT BLADE¿. THE TOOTH WAS RETRIEVED FROM THE PATIENT. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19850805 ↗