Mpower PRO6450MRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10845854012833), received between Mar 25, 2026 and Mar 25, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (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.

• MalfunctionMar 25, 2026Mechanical Problem

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE PRO6450M, MPOWER 2 BATTERY STERNUM SAW, WAS BEING USED ON 4FEB26 AND THE ¿SAW BLADE FALLS OFF MID CASE¿. PER FURTHER ASSESSMENT IT WAS REPORTED THE "SAW BLADE FELL OFF INTO THE SITE. WAS RETRIEVED.¿ THERE WAS NO REPORT OF IMPACT OR INJURY TO 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 24686317 ↗
• MalfunctionMar 25, 2026Mechanical Problem

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE PRO6450M, MPOWER 2 BATTERY STERNUM SAW, WAS BEING USED ON (B)(6) 2026 AND THE ¿SAW BLADE FALLS OFF MID CASE¿. PER FURTHER ASSESSMENT IT WAS REPORTED THE "SAW BLADE FELL OFF INTO THE SITE. WAS RETRIEVED.¿ THERE WAS NO REPORT OF IMPACT OR INJURY TO 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 24686316 ↗