Arthrex® AR-11390Recalls & reported problems
Arthrex, Inc. · PUNCH MENISCL RT TIP 2.75MM STR SFT · 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 00888867003187), received between Feb 1, 2021 and Feb 1, 2021 — classified as 1 malfunction.
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
- Mechanical Problem1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 1, 2021Mechanical Problem; Component Missing
IT WAS REPORTED THAT DURING A KNEE SURGERY THE BITING DEVICE STOPPED WORKING DIRECTLY IN THE JOINT CAVITY. THE DEVICE WAS REMOVED FROM THE JOINT, AND THE EXAMINATION REVEALED THAT THE WORKING PART OF THE PUNCH DOES NOT MOVE. IT WAS NOTICED THAT THERE IS NO SMALL PIN THAT FIXES THE WORKING PART OF THE PUNCH TO THE STATIONARY ONE. THE SURGEON LOOKED FOR THE PIN INSIDE THE KNEE JOINT BUT WAS NOT ABLE TO FIND THE MISSING PIN. IT IS LIKELY THAT THE PART REMAINED INSIDE THE PATIENT. THE SURGERY WAS THEN FINISHED SUCCESSFULLY WITH A DIFFERENT DEVICE AND THE SURGEON DID NOT SWITCH TO A DIFFERENT TECHNIQUE.
Patient problems: Foreign Body In Patient
MAUDE report 11258618 ↗
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.
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