Hall 50 PRO7400BRecalls & reported problems
Conmed Corporation · HALL 50 RECIPROCATING SAW BATTERY HANDPIECE · Class 1
Data updated Oct 13, 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 10845854040058), received between Apr 23, 2025 and Apr 23, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
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 23, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
A SALES REPRESENTATIVE REPORTED ON BEHALF OF A CUSTOMER THAT THE PRO7400B, HALL 50 RECIPROCATING SAW BATTERY HANDPIECE DEVICE WAS USED IN A TOTAL HIP PROCEDURE ON AN UNKNOWN DATE AND ¿THE SAW BLADE DETACHED FROM THE HANDPIECE TWO TIMES DURING ONE SURGERY. THE NURSE CAREFULLY ATTACHED THE SAW BLADE AFTER THE FIRST TIME BUT IT DETACHED AGAIN DURING ACTION DESPITE THAT. THE HANDPIECE WILL BE SENT FOR REPAIR. NO HARM CAME TO THE PATIENT AND THEY FINISHED THE SURGERY WITH ANOTHER HANDPIECE.". THE PROCEDURE WAS COMPLETED WITH ¿ANOTHER PRO7400B¿ AND A DELAY OF 5 MINUTES. FURTHER ASSESSMENT FOUND "THE BLADE CAME LOOSE DURING THE CUT OF COLLUM FEMORIS. THERE WERE NO PATIENT IMPACT OR INJURY. THERE WAS A MINIMAL DELAY IN THE SURGERY WHEN THEY OPENED A NEW HANDPIECE. THE TECHNICIANS IN THE HOSPITAL HAVE INVESTIGATED THE HANDPIECE AND CAN¿T FIND ANYTHING WRONG WITH IT. THEY HAVE DECIDED TO TRY THE SAW AGAIN DURING SURGERY AND NOT RETURNING IT TO US IF DOES NOT HAPPEN AGAIN. THE BLADE DETACHED ¿ THEY HAD TO STOP AND ATTACH THE BLADE AGAIN. THE SAME THING HAPPENED AGAIN WHEN THEY TRIED TO COMPLETE THE CUT. THEY THEN BROUGHT IN A DIFFERENT SAW AND COMPLETED THE OPERATION WITHOUT COMPLICATIONS. TH
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21889937 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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