HALL MICROPOWER+ PRO7000SERecalls & reported problems

Summary

The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 10845854040911), received between Jun 28, 2018 and Jul 7, 2025 — classified as 2 injuries, 11 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (10 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 13 most recent of 13 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 7, 2025Overheating of Device; Overheating of Device

  A CUSTOMER REPORTED THAT IN A NON-SURGICAL EVENT ON 16MAY25, THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL DEVICE ¿GETS HOT¿. THERE WAS NO REPORT OF INJURY, MEDICAL/SURGICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR ANY PATIENT OR USER. 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 22411850 ↗
• MalfunctionJul 1, 2025Overheating of Device; Overheating of Device

  A CUSTOMER REPORTED THAT IN A NON-SURGICAL EVENT ON APPROXIMATELY (B)(6) 2025, THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL DEVICE ¿GETS HOT¿. THERE WAS NO REPORT OF INJURY, MEDICAL/SURGICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR ANY PATIENT OR USER. 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 22370035 ↗
• MalfunctionJun 23, 2025Overheating of Device; Overheating of Device

  IT WAS REPORTED THAT, IN A NON-SURGICAL EVENT ON (B)(6) 2025, THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL DEVICE ¿GETS HOT¿. THERE WAS NO REPORT OF INJURY, MEDICAL/SURGICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR ANY PATIENT OR USER. 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 22306586 ↗
• MalfunctionJun 3, 2025Unstable; Unstable

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL DEVICE WAS BEING USED DURING A DENTAL PROCEDURE ON (B)(6) 2025 WHEN IT WAS REPORTED ¿THE HANDPIECE (WHIPPED) DURING USE ON THE PATIENT. PATIENT BONE WAS INADVERTENTLY DAMAGED AS A RESULT. I AM NOT SURE OF ANY FURTHER DETAILS; THIS IS THE ONLY INFORMATION I HAVE BEEN GIVEN.¿. THERE WAS NO REPORT OF MEDICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR THE PATIENT OR USER. THIS REPORT IS BEING RAISED ON THE REPORTED INJURY DUE TO THE PATIENT¿S BONE BEING DAMAGED.

  Patient problems: Insufficient Information

  MAUDE report 22135780 ↗
• MalfunctionFeb 4, 2025Overheating of Device; Overheating of Device

  THE DISTRIBUTOR REPORTED ON BEHALF OF THEIR CUSTOMER THAT THE DEVICE, PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL, WAS BEING USED DURING AN UNKNOWN PROCEDURE ON (B)(6) 2025 WHEN IT WAS REPORTED, ¿THE DEVICE IS OVERHEAT DURING OPERATION.¿ THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR HOSPITALIZATION FOR 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 21302721 ↗
• MalfunctionNov 12, 2024Overheating of Device; Overheating of Device

  A SALES REPRESENTATIVE REPORTED ON BEHALF OF A CUSTOMER THAT THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL DEVICE WAS USED IN AN UNNAMED PROCEDURE ON (B)(6) 2024, AND ¿THE DEVICE BURNS IN USE AND THEN STOPS WORKING.". IT WAS ALSO REPORTED THAT THERE WAS NO IMPACT TO A PATIENT OR USER. FURTHER ASSESSMENT FOUND THAT "THE EVENT DESCRIPTION SHOULD BE 'THE DEVICE WAS OVERHEATED DURING THE OPERATION'. NO FLAMES, SPARKS OR ARCING HAPPENED AND NEITHER A PATIENT OR USER BURNED NOR ANY MEDICAL/SURGICAL INTERVENTION OR EXTENDED HOSPITALIZATION INVOLVED IN THIS ISSUE." 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 20663859 ↗
• MalfunctionNov 11, 2024Overheating of Device; Overheating of Device

  A SALES REPRESENTATIVE REPORTED ON BEHALF OF A CUSTOMER THAT THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL WAS USED IN AN UNKNOWN PROCEDURE ON (B)(6) 2024, AND ¿THE DEVICE GETS HOT AND THEN STOPS WORKING¿. THERE WAS NO IMPACT TO ANY PATIENT OR USER. 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 20652333 ↗
• MalfunctionJul 8, 2024Overheating of Device; Overheating of Device

  CONMED CANADA REPORTED THAT THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL, DEVICE WAS FOUND ON 17JUN2024 WHEN IT WAS REPORTED ¿HANDPIECE NOISY AND GETTING HOT QUICK.¿. THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR THE PATIENT OR USER. 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 19690875 ↗
• MalfunctionMay 23, 2024Overheating of Device; Overheating of Device

  A SALES REPRESENTATIVE REPORTED ON BEHALF OF A CUSTOMER THAT THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL DEVICE WAS BEING USED DURING A UNILATERAL BIPORTAL ENDOSCOPIC SPINAL SURGERY PROCEDURE ON 17MAY24, AND ¿THE HANDLE WAS VERY HOT WHEN USED, AND THE HOST SCREEN REPORTED AN ERROR.¿. FOLLOW-UP ASSESSMENT FOUND THERE WAS NO INJURY TO THE PATIENT OR USER. THE PROCEDURE WAS COMPLETED WITH NO REPORTED DELAY. THERE WAS NO REPORT OF MEDICAL/SURGICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR 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 19380910 ↗
• MalfunctionMay 23, 2024Overheating of Device; Overheating of Device

  A SALES REPRESENTATIVE REPORTED ON BEHALF OF A CUSTOMER THAT THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL DEVICE WAS BEING USED DURING A UNILATERAL BIPORTAL ENDOSCOPIC SPINAL SURGERY PROCEDURE ON (B)(6) 2024, AND THE ¿PRO7000SE WAS HOT, REPORTED ERROR.¿. FOLLOW-UP ASSESSMENT FOUND THERE WAS NO INJURY TO THE PATIENT OR USER. THE PROCEDURE WAS COMPLETED WITH NO REPORTED DELAY. THERE WAS NO REPORT OF MEDICAL/SURGICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR 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 19380909 ↗
• MalfunctionMay 8, 2024Overheating of Device; Overheating of Device

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER, THAT THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL WAS BEING USED ON (B)(6) 2024 DURING AN UNKNOWN PROCEDURE WHEN IT WAS REPORTED ¿THE HANDLE IS HOT AND WON'T WORK.¿. THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR EXTENDED HOSPITALIZATION TO THE PATIENT OR USER. 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 19270714 ↗
• InjurySep 27, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL, WAS BEING USED DURING AN ORAL SURGERY PROCEDURE ON (B)(6) 2023 WHEN IT WAS REPORTED, ¿I WAS CALLED TO COLLECT A (REPAIR LOAN) HIGH SPEED DRILL THAT I WAS TOLD HAD BURNT A PATIENT. I INITIALLY SUSPECTED THAT I WOULD DISCOVER A BUR GUARD IN POOR CONDITION. ON INSPECTION I FOUND THE BUR GUARD TO BE IN EXCELLENT ORDER. THE TEST OF SPINNING THE BUR GUARD ON A BUR RESULTED IN AN EXTENDED FREE SPIN. I THEN DECIDED TO CONNECT THE DRILL, BUR GUARD AND EXAMPLE 3RD PARTY BUR (SAME AS THE INCIDENT) AND OPERATE THE DRILL AT 100,000 RPM TO SEE IF COULD REPLICATE THE OVER HEATING. WHILST THE DRILL MOTOR WARMED SLIGHTLY THE BUR GUARD NEVER WARMED AND CERTAINLY DID NOT GET HOT ENOUGH TO CAUSE A BURN. I SUSPECT THE BUR ITSELF CAUSED THE BURN THROUGH INATTENTION BY THE SURGEON. THE PATIENT RECEIVED A BURN TO THEIR LIP THAT REQUIRED "A STITCH" TO CLOSE THE WOUND.¿. THERE WAS NO REPORT OF HOSPITALIZATION FOR THE PATIENT AND THE PROCEDURE WAS COMPLETED. FURTHER ASSESSMENT QUESTIONING WAS ASKED; HOWEVER, TO DATE WE HAVE NOT RECEIVED ANY INDICATION OF DEGREE OF BURN OR FURTHER INFORMATION ON

  Patient problems: Burn(s)

  MAUDE report 17825531 ↗
• InjuryJun 28, 2018Device Issue; Device Issue

  THE CUSTOMER REPORTED THAT THE PRO7000SE, HALL MICROPOWER+ HIGH SPEED DRILL, WAS REPORTED TO HAVE BURNED A PATIENT DURING A TOOTH EXTRACTION ON (B)(6) 2018. THROUGH FURTHER RESEARCH WITH THE ACCOUNT IT WAS FOUND THAT THE DOCTOR LAID THE HANDPIECE BEING USED ON THE LIP OF THE PATIENT DURING THE PROCEDURE. THE FACILITY STATED THAT THEY WERE NOT AWARE THAT THE HANDPIECE COULD GET HOT. THE IFU OF THE HANDPIECE STATES THAT THE USER SHOULD CONTINUALLY CHECK FOR OVERHEATING DURING USE. THE CONTROLLER DEVICE, E9000, COMPLAINT (B)(4), HAS ALSO HAD A COMPLAINT REGISTERED SINCE IT WAS INVOLVED IN THE PROCEDURE. THERE WAS NO FAILURE MODE LISTED FOR THE CONTROLLER OR THE HANDPIECE, ONLY THAT THEY WERE INVOLVED WITH THE PATIENT BURN. THIS REPORT IS BEING RAISED ON THE BASIS OF INJURY DUE TO THE BURN DEGREE BEING UNKNOWN.

  Patient problems: Burn(s)

  MAUDE report 7647843 ↗