HALL 00507112900Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10845854003770), received between Feb 10, 2022 and May 26, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Material Fragmentation” (4 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 26, 2026Material Fragmentation

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE DEVICE 00507112900, LARGE BONE, HALL BLADE, OSCILLATING, 19.5 X 105 X 1.27 WAS BEING USED AND THERE WAS A ¿BROKEN SAW BLADE¿ THERE WAS NO IMPACT OR INJURY TO THE PATIENT OR USER. PER FURTHER ASSESSMENT IT WAS REPORTED THAT THE DEVICE FRAGMENTS FELL INTO THE SURGICAL SITE AND WERE RETRIEVED. 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 25280044 ↗
• MalfunctionFeb 20, 2026Material Fragmentation

  THE CUSTOMER REPORTED THAT THE THAT THE 00507112900 LARGE BONE, HALL BLADE, OSCILLATING, 19.5 X 105 X 1.27, DEVICE WAS BEING USED ON AN UNKNOWN DATE DURING AN UNKNOWN PROCEDURE WHEN IT WAS REPORTED ¿WE HAD ONE 5071-129 BLADE BREAK.¿. FURTHER ASSESSMENT FOUND THAT THE DEVICE DID FRAGMENT INTO THE SURGICAL SITE AND WAS REMOVED. THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR THE PATIENT OR USER. 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 24399682 ↗
• MalfunctionFeb 25, 2022Material Fragmentation; Material Fragmentation

  THE CUSTOMER REPORTED THAT THE DEVICE, 00507112900, LARGE BONE HALL BLADE WAS BEING USED ON (B)(6) 2022 DURING AN UNKNOWN PROCEDURE AND THE ¿DISTAL TIP BREAKING OFF DURING PROCEDURE NO INJURIES DELAYS OF 5 MINS WAS RETRIEVED¿. THERE WAS NO INJURY OR IMPACT TO THE PATIENT. THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13600800 ↗
• MalfunctionFeb 10, 2022Material Fragmentation; Material Fragmentation

  THE CUSTOMER REPORTED THAT THE DEVICE, 00507112900, LARGE BONE HALL BLADE WAS BEING USED ON (B)(6) 2022 DURING AN UNKNOWN PROCEDURE AND ¿WHILE USING HALL POWER OSC SAW THE LARGE BONE BLADE BROKE AND CRACKED ON SECOND BLADE¿. THERE WAS NO INJURY OR IMPACT TO THE PATIENT. THE PROCEDURE WAS COMPLETED WITH A DIFFERENT BLADE. THERE WAS A 15 MINUTE DELAY TO THE PROCEDURE. FURTHER ASSESSMENT FOUND THAT THE DEVICE DID FRAGMENT AND ALL PIECES WERE RETRIEVED WITH A HEMOSTAT. THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13506270 ↗