HALLRecalls & reported problems across all models
Conmed Corporation · 5 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 32
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls
- 0
We found 5 models of HALL by Conmed Corporation in the FDA's device registry (GUDID). Together they are named in 32 adverse event reports in the FDA's MAUDE database, received between Feb 10, 2022 and May 26, 2026 — classified as 2 injuries, 30 malfunctions.
The most frequently reported specific device problem is “Overheating of Device” (24 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported HALL problems
Device problems
- Overheating of Device24
- Material Fragmentation7
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions30
- Burn(s)2
HALL models
5 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Hall PRO7000DESAW, POWERED, AND ACCESSORIES24 reports
- HALL 00507112900BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL4 reports
- HALL® 00507126700BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL2 reports
- HALL® 00507125500BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL1 report
- HALL L3500SBBATTERY, REPLACEMENT, RECHARGEABLE1 report
Recent HALL adverse event reports
The 15 most recent reports across all models, 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 ↗MalfunctionDec 16, 2025Overheating of Device; Overheating of Device
A DISTRIBUTOR REPORTED ON BEHALF OF A CUSTOMER THAT THE PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL DEVICE WAS IN USE DURING PRE-OPERATIVE TESTING ON AN UNKNOWN DATE, AND ¿THIS HANDPIECE IS FOUND TO HAVE WEIRD NOISE AND OVER-HEATED OF THE MOTOR WHILE IT IS BEING USED.¿. 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 23815324 ↗MalfunctionOct 1, 2025Overheating of Device; Overheating of Device
A CUSTOMER REPORTED THAT THE PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL DEVICE WAS OBSERVED IN PRE-OPERATIVE TESTING ON APPROXIMATELY (B)(6) 2025, AND ¿BUR LOCK, OVER HEATED, NOT CONNECTING¿ WAS FOUND. 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 23189302 ↗MalfunctionJun 23, 2025Overheating of Device; Overheating of Device
A CUSTOMER REPORTED THAT THE PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL DEVICE WAS FOUND TO BE ¿RUNNING HOT¿ IN PRE-OPERATIVE TESTING ON AN UNKNOWN DATE. 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 22306483 ↗MalfunctionJun 12, 2025Overheating of Device; Overheating of Device
THE CUSTOMER REPORTED THAT THE THAT PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL DEVICE WAS FOUND DURING A NON-SURGICAL PROCEDURE ON APPROXIMATELY (B)(6) 2025 WHEN IT WAS REPORTED ¿GETS TOO HOT.¿. 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 22193864 ↗MalfunctionApr 16, 2025Overheating of Device; Overheating of Device
DURING A REQUEST FOR SERVICE MADE ON (B)(6) 2025, A CUSTOMER REPORTED THAT THE PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL DEVICE WAS ¿GETTING HOT¿. FURTHER ASSESSMENT FOUND THIS EVENT OCCURRED DURING AN UNNAMED PATIENT PROCEDURE ON AN UNKNOWN DATE. THERE WAS NO INJURY 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 21851469 ↗MalfunctionMar 7, 2025Overheating of Device; Overheating of Device
A CUSTOMER REPORTED THAT THE PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL WAS USED IN AN UNNAMED PROCEDURE ON AN UNKNOWN DATE AND BECAME ¿NOISY AND HOT¿. THE PROCEDURE WAS COMPLETED WITH A ¿NEW HANDPIECE¿, AND WITH NO DELAY ¿EXCEPT TO GET THE ALTERNATE DEVICE¿, WHICH WAS NEARBY. THERE WAS NO REPORT OF INJURY, MEDICAL/SURGICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR THE PATIENT OR USER. THE CUSTOMER WAS UNABLE TO PROVIDE FURTHER DETAILS ABOUT THE EVENT. 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 21546339 ↗MalfunctionFeb 21, 2025Overheating of Device; Overheating of Device
THE CUSTOMER REPORTED THAT THE DEVICE PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL, WAS BEING USED ON APPROXIMATELY (B)(6) 2025 AND "GETS HOT¿. THERE WAS NO IMPACT OR INJURY 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 21434127 ↗MalfunctionFeb 18, 2025Overheating of Device; Overheating of Device
THE CUSTOMER REPORTED THAT THE PRO7000DE, HALL ORALMAX ELITE HIGH-SPEED DRILL, DEVICE WAS BEING USED ON APPROXIMATELY (B)(6) 2025 DURING A NON-SURGICAL EVENT WHEN IT WAS REPORTED ¿LOUD HOT.". THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, EXTENDED 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 21401416 ↗MalfunctionFeb 10, 2025Overheating of Device; Overheating of Device
A CUSTOMER REPORTED THAT THE PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL DEVICE WAS ¿NOISY AND HOT¿ IN A NON-SURGICAL EVENT ON 28JAN25. THERE WAS NO PATIENT INVOLVEMENT AND NO REPORT OF INJURY OR IMPACT TO ANY 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 21343156 ↗MalfunctionFeb 6, 2025Overheating of Device; Overheating of Device
THE CUSTOMER REPORTED THAT THE PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL, DEVICE WAS BEING USED ON A 16JAN25 DURING AN UNKNOWN PROCEDURE WHEN IT WAS REPORTED ¿GETS HOT.". THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, EXTENDED 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 21321003 ↗MalfunctionFeb 3, 2025Overheating of Device; Overheating of Device
THE CUSTOMER REPORTED THAT THE DEVICE PRO7000DE HALL ORALMAX ELITE HIGH SPEED DRILL, WAS BEING USED ON APPROXIMATELY (B)(6) 2025 AND WAS ¿GETTING HOT¿. THERE WAS NO IMPACT OR INJURY 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 21292526 ↗MalfunctionJan 23, 2025Overheating of Device; Overheating of Device
THE CUSTOMER REPORTED THAT THE DEVICE PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL, WAS BEING USED ON (B)(6) 2025 AND IT "GETS HOT".THERE WAS NO IMPACT OR INJURY FOR THE PATIENT OR USER. THE SURGERY WAS COMPLETED WITH NO DELAY. 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 21216899 ↗MalfunctionDec 17, 2024Overheating of Device; Overheating of Device
THE CUSTOMER REPORTED THAT THE DEVICE, PRO7000DE, HALL ORALMAX ELITE HIGH SPEED DRILL, WAS BEING USED DURING AN UNKNOWN PROCEDURE ON AN UNKNOWN DATE WHEN IT WAS REPORTED, ¿THE DEVICE IS NOT CUTTING TOOTH/BONE AND GETS VERY HOT DURING USE.¿. THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR HOSPITALIZATION FOR THE PATIENT OR THE 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 20950477 ↗
Other Conmed Corporation products
All Conmed Corporation devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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