N/A 3865DRecalls & reported problems
Smith & Nephew, Inc. · REFURB CANNULA 2.2 FOR 1.9 SCOPES · 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 00885556504437), received between Aug 18, 2017 and Aug 18, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Metal Shedding Debris” (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
- Metal Shedding Debris1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2017Metal Shedding Debris
IT WAS REPORTED THAT A METAL FLAKES SHED FROM THE CANNULA DURING WRIST ARTHROSCOPY, METAL FLAKES SHED INSIDE OF THE PATIENT AND REMOVED BY FLUSHING AS MUCH AS POSSIBLE. HEALTH CARE PROFESSIONAL WAS ABLE TO COMPLETE THE PROCEDURE WITH THE SAME DEVICE AND WITHOUT A BACK-UP DEVICE. AFTER THE OPERATION, PATIENT WAS X-RAYED AND NO METAL FLAKES WERE OBSERVED, CONSEQUENTLY, THERE IS EVIDENCE OF NO PATIENT INJURIES OR COMPLICATIONS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6805878 ↗
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- 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.
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