Dry-Doc C7360Recalls & reported problems
Conmed Corporation · DRY-DOC CANNULA WITH DISPOSABLE OBTURATOR, 7.0 X 85 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 10845854020050), received between Nov 19, 2020 and Nov 19, 2020 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component1
- 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.
MalfunctionNov 19, 2020Material Fragmentation; Detachment of Device or Device Component; Material Fragmentation; Detachment of Device or Device Component
CONMED (B)(6) RECEIVED A REPORT FROM THE DISTRIBUTOR DOCUMENTING ISSUES INVOLVING THE C7360, DRY-DOC CANNULA WITH DISPOSABLE OBTURATOR 7.0 X 85MM, LOT 1079066, OCCURRING ON (B)(6) 2020. IT WAS NOTED THAT DURING A ROTATOR CUFF REPAIR, IN THE MIDDLE OF INSERTING A SCORPION INTO ANTERIOR PORTAL, THE END CAP WAS DETACHED FROM THE CANNULA BODY. THE DETACHED END CAP WAS REMOVED USING A GRASPER AND RETRIEVER FORCEPS. THE SURGERY WAS COMPLETED SUCCESSFULLY USING A C7312 WITH A 4-MINUTE DELAY. THE INFORMATION RECEIVED NOTED THE PATIENT WAS A (B)(6) YEAR OLD FEMALE AND THERE WAS NO IMPACT, OR INJURY TO HER. ADDITIONAL INFORMATION INDICATES WHEN THE INSTRUMENT WENT BACK AND FORTH, THE WATER LEAKED AS THE CANNULA AND SEAL WERE IN ACROMIOM. THE SEAL BECAME DETACHED FROM THE CANNULA. IT TOOK ABOUT 4 MINS TO FIND IT INSIDE OF THE PATIENT'S BODY, BUT WAS REMOVED COMPLETELY. IT WAS CONFIRMED THE PATIENT'S CONDITION IS GOOD. THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE (FRAGMENTATION IN THE PATIENT BUT REMOVED).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10867642 ↗
Other Accessories, arthroscopic devices
- Arthrex® AR-12990Arthrex, Inc. · Accessories, arthroscopic409 reports
- NA 228302Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC287 reports
- FIRSTPASS 72290128Smith & Nephew, Inc. · ACCESSORIES,ARTHROSCOPIC232 reports
- NA 251723Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC145 reports
- COBRA 3910900093Stryker Corporation · Accessories, arthroscopic138 reports
- FirstPass 72290129Smith & Nephew, Inc. · Accessories, arthroscopic82 reports
- FirstPass 72290130Smith & Nephew, Inc. · Accessories, arthroscopic80 reports
- MITEK 242025Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC61 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page