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Shoulder Innovations Inset Reverse Total Shoulder RSA 24mm Angled Reamer (0 deg)Recalls & reported problems

Shoulder Innovations, Inc. · Shoulder Innovations Inset Reverse Total Shoulder - RSA 24mm Angled Reamer (0 deg) · Class 2 · Implant

Data updated Oct 18, 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 B1132R2GR400240), received between Jan 13, 2023 and Jan 13, 2023 — classified as 1 injury.

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

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Limb Fracture1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 13, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    GLENOID FRACTURE DURING USE OF 24MM X 0° ANGLED REAMER.

    Patient problems: Limb Fracture

    MAUDE report 16165173 ↗

Other Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented devices

All Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented devices →

Sources and updates

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