CONMED C7313Recalls & reported problems
Conmed Corporation · CLEAR FLEXIBLE CANNULA, 6.5 MM X 73 MM · 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 10845854019948), received between Mar 19, 2026 and Mar 19, 2026 — classified as 1 malfunction.
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.
MalfunctionMar 19, 2026Material Fragmentation
THE CUSTOMER REPORTED THAT THE DEVICE, C7313, CLEAR FLEXIBLE CANNULA, 6.5 MM X 73 MM, WAS USED DURING AN UNKNOWN PROCEDURE ON 4MAR26 WHEN IT WAS REPORTED, ¿DURING THE SURGERY, IT APPEARED THAT A PIECE OF SEALING BECAME DETACHED INSIDE THE CANNULA. THE DETACHED FRAGMENT ENTERED THE SURGICAL SITE AND WAS REMOVED USING A GRASPER. AFTER REMOVAL, IT WAS CONFIRMED THAT NO FRAGMENTS REMAINED INSIDE THE PATIENT. BOTH THE REMOVED FRAGMENT AND THE DEVICE WERE IMMEDIATELY DISCARDED IN THE OPERATING ROOM AND ARE NOT RETRIEVABLE.¿. THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR HOSPITALIZATION FOR THE PATIENT. THE PROCEDURE WAS COMPLETED WITH AN ALTERNATE DEVICE CAUSING A 5-MINUTE 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 24637088 ↗
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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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