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Arthrex® AR-11851SRRecalls & reported problems

Arthrex, Inc. · RHINO, RIGHT CURVE TIP, WITH SR HANDLE · 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 00888867003682), received between Mar 29, 2018 and Mar 29, 2018 — classified as 1 injury.

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 16, 2026.

Most reported problems

Device problems

  • Break1
  • Detachment Of Device Component1

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.

  • InjuryMar 29, 2018Break; Detachment Of Device Component

    IT WAS REPORTED THAT THE TIP OF THE DEVICE BROKE DURING SHOULDER SURGERY. IT WAS NOT POSSIBLE TO REMOVE THE BROKEN FRAGMENT. THE SURGERY WAS COMPLETED SUCCESSFULLY WITH A NEW DEVICE OF THE SAME PART NUMBER.

    Patient problems: Foreign Body In Patient

    MAUDE report 7380851 ↗

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Sources and updates

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