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INHANCE 5503-00-025Recalls & reported problems

Depuy (Ireland) · INHANCE SHOULDER SYSTEM NON-LOCKING SCREW 25mm · Class 2 · Implant

All models of INHANCE (202)

Data updated Oct 18, 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 10603295546856), received between Nov 18, 2022 and Nov 18, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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 18, 2026.

Most reported problems

Device problems

  • Difficult to Insert1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionNov 18, 2022Difficult to Insert; Difficult to Insert

    IT WAS REPORTED THAT SURGEON WAS PLANNING TO USE A NON-LOCKING SCREW TO ACHIEVE COMPRESSION OF THE SMALL BASEPLATE. WHEN INSERTING THE 25MM NON-LOCKING SCREW, THE SCREW WENT DIRECTLY THROUGH THE BASEPLATE PERIPHERAL HOLE. THERE WAS 10 MINS OF SURGICAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15824867 ↗

Other PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED devices

All PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED devices →

Sources and updates

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