Arthrex® AR-3355-2730Recalls & reported problems
Arthrex, Inc. · C-MOUNT AR-SCOPE,30°2.7X 72MM LGTH · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00888867029835), received between Aug 10, 2021 and Aug 22, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Crack1
- Scratched Material1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 22, 2024Crack; Crack
ON 07/30/2024, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA (B)(4) THAT AN AR-3355-2730 SCOPE IS DAMAGED. A DOCTOR WAS ATTEMPTING TO DO AN ANKLE SCOPE AND HIT THE SCOPE WITH A BURR. THE SCOPE IS NOW CRACKED. THIS OCCURRED DURING USE IN A CASE WITH NO PATIENT EFFECT. ANOTHER DEVICE WAS USED TO COMPLETE THE CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20038635 ↗MalfunctionJul 14, 2023Scratched Material; Scratched Material
ON 6/16/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS THAT AN AR-3355-2730 SCOPE LENS WAS SCRATCHED. THIS WAS DISCOVERED DURING AN ARTHROSCOPIC PROCEDURE. THE CASE WAS COMPLETED BY USING A NEW SCOPE WITH NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17329777 ↗MalfunctionAug 10, 2021Break
IT WAS REPORTED THE AR-3355-2730 SCOPE IS DAMAGED. ADDITIONAL INFORMATION ON 7/21/2021: IT WAS REPORTED BY THE SALES REP, THAT DURING AN ANKLE PROCEDURE ON (B)(6) 2021 WITH DR. HULL. THE SURGEON WAS USING AR-3355-2730 C-MOUNT 2.7 SCOPE, AFTER INSERTION, THE SHAFT BROKE WHEN THE SURGEON WAS TRYING TO LOOK DEEP INSIDE THE ANKLE JOINT, UNDER THE TALUS. THE BROKEN PIECE WAS REMOVED. THE CASE WAS COMPLETED USING A BACK UP AR-3355-2730 C-MOUNT 2.7 SCOPE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12300620 ↗
Other ARTHROSCOPE devices
- FMS 283512Medos International Sàrl · ARTHROSCOPE1,800 reports
- Arthrex® AR-6480Arthrex, Inc. · ARTHROSCOPE949 reports
- FMS VUE 284002Depuy Mitek, LLC · ARTHROSCOPE829 reports
- MITEK 242018Medos International Sàrl · Arthroscope731 reports
- METRx® System 9560100Medtronic Sofamor Danek, Inc. · Arthroscope667 reports
- FMS VUE II 284004Medos International Sàrl · Arthroscope562 reports
- VAPR COOLPULSE 228146Depuy Mitek, LLC · ARTHROSCOPE474 reports
- FMS DUO 284580Depuy Mitek, LLC · ARTHROSCOPE458 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 18, 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