PowerPro PRO6045Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10845854028605), received between Jun 8, 2022 and Sep 26, 2024 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

• MalfunctionSep 26, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE PRO6045, HALL SURGICAL POWERPRO RECIPROCATING SAW ATTACHMENT WAS BEING USED ON (B)(6) 2024 AND ¿THE INCIDENTS HAPPENED DURING A POWER TRIAL, 2 TOTAL HIP SURGERIES. THE ATTACHMENT (PRO6045) DETACHED FROM THE HAND PIECE¿ONE TIME DURING THE SECOND PROCEDURE. THE ATTACHMENT DETACHED WHEN IT WAS PUT UNDER PRESSURE, DURING THE CUT WHEN REMOVING CAPUT. NO HARM CAME TO THE STAFF OR PATIENT.¿. PER FURTHER ASSESSMENT IT WAS FOUND THAT "THE ATTACHMENT DETACHED WHEN IT WAS USED TO CUT COLLUM DURING A TOTAL HIP SURGERY. SO, THE PRO6045 WITH SAWBLADE (5052-261) WAS IN THE WOUND WHEN IT CAME OFF¿THE SAME THING HAPPENED ONE TIME AT THE SECOND SURGERY. ¿THE PRO6045 CAME OFF IN ONE PIECE. NO COMPONENTS FELL OFF FROM THE PRO6045 ITSELF OR THE PRO9200B.¿. THE PROCEDURE WAS COMPLETED WITHOUT AN ALTERNATE DEVICE. THERE WAS A MINUTE DELAY. THE PRO9200B, HALL TITAN DUAL TRIGGER BATTERY HANDPIECE WILL BE LISTED AS A CONCOMITANT DEVICE AND THERE WAS NO ALLEGATION AGAINST IT. 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 20309759 ↗
• MalfunctionSep 26, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE PRO6045, HALL SURGICAL POWERPRO RECIPROCATING SAW ATTACHMENT WAS BEING USED ON 9SEP2024 AND ¿THE INCIDENTS HAPPENED DURING A POWER TRIAL, 2 TOTAL HIP SURGERIES. THE ATTACHMENT (PRO6045) DETACHED FROM THE HAND PIECE 2 TIMES¿THE ATTACHMENT DETACHED WHEN IT WAS PUT UNDER PRESSURE, DURING THE CUT WHEN REMOVING CAPUT. NO HARM CAME TO THE STAFF OR PATIENT.". PER FURTHER ASSESSMENT IT WAS FOUND THAT "THE ATTACHMENT DETACHED WHEN IT WAS USED TO CUT COLLUM DURING A TOTAL HIP SURGERY. SO, THE PRO6045 WITH SAWBLADE (5052-261) AS IN THE WOUND WHEN IT CAME OFF. IT HAPPENED 2 TIMES DURING THIS STEP AT THE FIRST SURGERY, BUT THE SURGEON WAS ABLE TO REATTACH IT TO THE HANDPIECE AND COMPLETE THE CUT. ¿THE PRO6045 CAME OFF IN ONE PIECE. NO COMPONENTS FELL OFF FROM THE PRO6045 ITSELF OR THE PRO9200B.". THE PROCEDURE WAS COMPLETED WITHOUT AN ALTERNATE DEVICE. THERE WAS A MINUTE DELAY. THE PRO9200B, HALL TITAN DUAL TRIGGER BATTERY HANDPIECE WILL BE LISTED AS A CONCOMITANT DEVICE AND THERE WAS NO ALLEGATION AGAINST IT. 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 20309685 ↗
• MalfunctionMar 30, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

  THE DISTRIBUTOR REPORTED ON BEHALF OF THE CUSTOMER THAT THE PRO6045 POWERPRO RECIPROCATING SAW ATTACHMENT, WAS BEING USED DURING A UKA PROCEDURE ON THE DATE OF (B)(6) 2023, WHEN IT WAS REPORTED, ¿ IT WAS REPORTED THAT PRO6045 POWERPRO RECIPROCATING SAW ATTACHMENT CAME OFF PRO9100B HALL TITAN SINGLE TRIGGER HANDPIECE WHEN THIS ATTACHMENT WAS ATTACHED TO THIS HANDPIECE AND THE BONE WAS CUT WHILE PULLING THIS HANDPIECE TOWARD SURGEON SIDE. L3000LG LARGE LITHIUM BATTERY WAS USED AS THE BATTERY.¿ AFTER FURTHER ASSESSMENT, IT WAS REPORTED THAT A DETACHMENT OF THE DEVICE OCCURRED WHILE IN USE OF CUTTING THE BONE, BUT IT WAS RETRIEVED WITH A FORCEP INSTRUMENT AND THERE WAS NO INJURY TO THE PATIENT. THE PRO9100B, HALL TITAN SINGLE TRIGGER BATTERY HANDPIECE AND THE L3000LG LARGE LITHIUM BATTERY ARE BOTH LISTED AS CONCOMITANT DEVICES AND HAD NO ALLEGATIONS AGAINST THEM. IT IS UNKNOWN IF THERE WAS ANY DELAY AND AN ALTERNATIVE DEVICE WAS NOT USED. THERE WAS NO PATIENT OR USER IMPACT, PROLONGED HOSPITALIZATION, OR MEDICAL/ SURGICAL INTERVENTION. 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 16642671 ↗
• MalfunctionJun 8, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE PRO6045, HALL SURGICAL POWERPRO RECIPROCATING SAW ATTACHMENT, WAS USED IN AN UNKNOWN TYPE OF PROCEDURE ON (B)(6) 2022 WHEN IT WAS REPORTED ¿HANDPIECE AND ATTACHMENT DO NOT FIT PROPERLY. DON¿T KNOW IF IT IS THE ATTACHMENT OR THE HANDPIECE THAT HAVE THE ISSUE. THE ATTACHMENT GETS LOOSE DURING SURGERY DUE TO A LOT OF VIBRATIONS AND/OR THAT THE ATTACHMENT DO NOT FIT PROPERLY (IT IS LOOSE). HIGHT NOISE AND ATTACHMENT DID LOOSE COMPLETELY AND WAS FOUND ON THE PATIENT. NO DAMAGE WAS MADE, BUT VERY CLOSE TO PATIENT DAMAGE. THE PROCEDURE WAS COMPLETED AS PLANNED WITHOUT AN ALTERNATE DEVICE. THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR HOSPITALIZATION FOR THE PATIENT. FURTHER ASSESSMENT QUESTIONING FOUND THAT THE ATTACHMENT HAD A SAWBLADE ATTACHED. THE COMPONENT WAS TAKEN OUT OF THE SURGICAL SITE BY THE NURSE. THE PRO9200B, HALL TITAN DUAL TRIGGER BATTERY HANDPIECE, WAS THE CONCOMITANT DEVICE USE WITH THE ATTACHMENT. 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 14630681 ↗