Hall® Titan™ PRO9200BRecalls & reported problems
Conmed Corporation · HALL TITAN DUAL TRIGGER BATTERY HANDPIECE · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 40845854050836), received between Apr 8, 2024 and Apr 8, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Self-Activation or Keying” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Self-Activation or Keying1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 8, 2024Self-Activation or Keying; Self-Activation or Keying
A SALES REPRESENTATIVE REPORTED ON BEHALF OF A CUSTOMER THAT THE PRO9200B, HALL TITAN DUAL TRIGGER BATTERY HANDPIECE DEVICE WAS BEING USED DURING A REVERSE TOTAL SHOULDER ARTHROPLASTY PROCEDURE ON (B)(6) 2024, AND ¿TITAN DRILL SPINNING ON OWN¿. FURTHER ASSESSMENT FOUND THAT THE SURGEON "STOPPED DRILLING AND THEN THE DRILL STARTED SPINNING ON ITS OWN", AND "THE BATTERY THAT WAS IN USE HAD A PARTIALLY ERODED POSISITVE TERMINAL. IT WAS ALSO TAKEN OUT OF SERVICE". ADDITIONALLY, THE SALES REPRESENTATIVE STATED "NO REASON TO BELIEVE IT WAS THE BATTERY OR A MANUFACTURING ISSUE, THEY WAS OLD AND WHEN I LOOKED AT IT IT HAD ALLOT OF CORROSION FROM POOR UPKEEP".THE PROCEDURE WAS COMPLETED WITH AN UNNAMED ALTERNATE DEVICE AND A DELAY OF 5 MINUTES. THERE WAS NO REPORT OF INJURY, 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. THE DEVICE L3000LG, HALL LARGE LITHIUM BATTERY WAS USED DURING THIS REPORTED EVENT AND WILL BE LISTED AS A CONCOMITANT DEVICE; THERE IS NO ALLEGATION AGAINST IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19060816 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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