INHANCE 6105-30-050Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295538943), received between Nov 25, 2025 and May 29, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 29, 2026Break

  IT WAS REPORTED THAT THE LARGE CIRCLE REAMER BROKE ON THE GLENOID.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25336933 ↗
• MalfunctionNov 25, 2025Break; Break

  IT WAS REPORTED DURING SURGERY, THE SURGEON WAS REAMING THE GLENOID AND WHEN TAKING THE REAMER OUT, NOTICED THE TIP OF THE LARGE CIRCULAR GLENOID REAMER WAS BROKEN OFF. THE BROKEN TIP WAS RETRIEVED FROM WITHIN THE PATIENTS GLENOID AND THE CASE CARRIED ON AS NORMAL. THERE WAS A VERY SHORT DELAY WHEN RETRIEVING THE BROKEN TIP FROM THE PATIENT'S GLENOID. NO ADDITIONAL DELAYS OR ADVERSE EVENTS TOOK PLACE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23643166 ↗