Arthrex® AR-11910NRRecalls & reported problems
Arthrex, Inc. · GRSPR,MINI,2.75 MM 15°UP CRV W/NR HNDL · 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 00888867003842), received between Jun 21, 2017 and Jun 21, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Component Missing” (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
- Component Missing1
- Device Or Device Fragments Location Unknown1
- Difficult to Open or Close1
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.
InjuryJun 21, 2017Component Missing; Device Or Device Fragments Location Unknown; Difficult to Open or Close
IT WAS REPORTED VIA MEDWATCH (B)(4) THAT DURING A NON-UNION OF BONE AFTER ORIF (OPEN REDUCTION INTERNAL FIXATION) OF ANKLE A SCREW OR PIN FROM THE 2.75 MM 15° CURVED MINI GRASPER WAS MISSING. DURING THE PROCEDURE THE SURGEON WAS ATTEMPTING TO OPEN THE GRASPER IN THE PATIENT'S ANKLE JOINT, BUT THE JAWS OF THE INSTRUMENT WOULD NOT OPEN. THE INSTRUMENT WAS TAGGED AND SENT TO SPD (STERILE PROCESSING DEPARTMENT). AFTER SPD CLEANED AND INSPECTED THE INSTRUMENT, IT WAS FOUND THAT EITHER A SET PIN OR TINY SCREW WAS MISSING FROM THE JAWS OF THE INSTRUMENT. THE PATIENT HAD AN X-RAY PERFORMED AT THE NEXT VISIT AND NO METAL OR RETAINED FOREIGN OBJECT WAS NOTED. UNCLEAR WHAT HAPPENED WITH THE SCREW.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6656256 ↗
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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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