MINI-REVO C6114Recalls & reported problems
Conmed Corporation · MINI-REVO BONE PUNCH, 1.5 MM · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854030745), received between Jul 1, 2024 and Jul 1, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Material Fragmentation” (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
- Material Fragmentation1
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.
InjuryJul 1, 2024Material Fragmentation; Material Fragmentation
THE CUSTOMER REPORTED THAT THE C6114, MINI-REVO BONE PUNCH 1.5MM, DEVICE WAS BEING USED DURING AN UNKNOWN PROCEDURE ON (B)(6) 2024 WHEN IT WAS REPORTED ¿INSTRUMENT PURCHASED THROUGH CONMED THAT BROKE OFF IN THE PATIENT. WE DID TAKE THE PATIENT BACK TO SURGERY TO RETRIEVE THE PIECE ON THE SAME DAY AND SHE IS DOING FINE.¿. THE PROCEDURE WAS COMPLETED AND THERE WAS NO REPORT OF EXTENDED HOSPITALIZATION FOR THE PATIENT OR USER. THIS REPORT IS BEING RAISED ON THE REPORTED INJURY DUE TO THE PATIENT BEING TAKEN BACK TO SURGERY TO REMOVE A FOREIGN BODY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19646176 ↗
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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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