Hall® Titan™ PRO9300BRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 40845854050799), received between Aug 10, 2022 and Dec 12, 2023 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 12, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER, THAT THE PRO9300B, HALL TITAN OSCILLATING SAW BATTERY HANDPIECE WAS BEING USED DURING AN UNKNOWN PROCEDURE ON (B)(6) 2023 WHEN IT WAS REPORTED ¿SAW CAME APART.¿THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION OR EXTENDED HOSPITALIZATION TO THE PATIENT OR USER. THIS REPORT IS BEING RAISED ON THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18310768 ↗
• MalfunctionFeb 8, 2023Material Fragmentation; Material Fragmentation

  THE DISTRIBUTOR REPORTED ON BEHALF OF THE CUSTOMER THAT THE PRO9300B, HALL TITAN OSCILLATING SAW BATTERY HANDPIECE, WAS BEING USED DURING A TKA PROCEDURE ON THE DATE OF (B)(6) 2023 WHEN IT WAS REPORTED, ¿THE OSCILLATOR HEAD OF THE MAIN BODY WAS CUT OFF DURING OSTEOTOMY USING THIS HALL TITAN OSCILLATOR.¿. AFTER FURTHER ASSESSMENT, IT WAS REPORTED THE DEVICE DID FRAGMENT IN THE SURGICAL SITE. THE FRAGMENT WAS RETRIEVED WITH A ¿FORCEP LIKE¿ INSTRUMENT. THE PATIENTS STATUS IS REPORTED TO BE IN GOOD STANDING. THE PROCEDURE WAS COMPLETED WITH A BACK UP INSTRUMENT AND NO REPORT OF MEDICAL INTERVENTION, OR PROLONGED 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 16324754 ↗
• MalfunctionAug 10, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  THE DISTRIBUTOR REPORTED ON BEHALF OF THEIR CUSTOMER THAT THE PRO9300B, HALL TITAN OSCILLATING SAW BATTERY HANDPIECE, WAS BEING USED DURING A TKA SURGERY, WHEN A FEMORAL OSTEOTOMY WAS PERFORMED, ON (B)(6) 2022 WHEN IT WAS REPORTED, ¿THE CUSTOMER REPORTED THAT THE LOWER PART OF THE OSCILLATOR HEAD TURNED AND FELL OFF WHILE USING THIS HANDPIECE.¿ THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR HOSPITALIZATION FOR THE PATIENT. THE PROCEDURE WAS REPORTED AS BEING COMPLETED WITH ALTERNATE, BACKUP INSTRUMENTS. FURTHER ASSESSMENT QUESTIONING WAS ASKED, AND IT WAS FOUND THAT THE OSCILLATING HEAD COMPONENT FELL INTO THE SURGICAL SITE AND WAS REMOVED WITH FORCEPS. 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 15197168 ↗