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GLOBAL UNITE 1100-20-300Recalls & reported problems

Depuy (Ireland) · GLOBAL UNITE COLLAR STANDARD SIZE48 · Class 2 · Implant

All models of GLOBAL UNITE (91)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295004264), received between Dec 5, 2017 and Feb 9, 2018 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

8 other recalls cover devices cleared under the same FDA submission (K101996, K170748); they may or may not involve this specific model.

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
  • Insufficient Device Problem Information1

Patient problems

  • Unspecified Infection2

Recent adverse event reports

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

  • InjuryFeb 9, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

    THE PATIENT WAS REVISED TO ADDRESS INFECTION. DOI: (B)(6) 2017; DOR: (B)(6) 2017; RIGHT SHOULDER.

    Patient problems: Unspecified Infection

    MAUDE report 7259007 ↗
  • InjuryDec 5, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    PATIENT WAS REVISED TO ADDRESS INFECTION AND LOOSENING OF THE UNKNOWN COMPONENT AT BONE TO CEMENT INTERFACE, DEPUY CEMENT WAS USED.

    Patient problems: Unspecified Infection

    MAUDE report 7084616 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K101996, K170748. One submission often covers many models, so check the product and lot details in each record.

  • Z-0487-2022 · Dec 7, 2021 · Terminated
    GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600
  • Z-0489-2022 · Dec 7, 2021 · Terminated
    GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100
  • Z-0483-2022 · Dec 7, 2021 · Terminated
    GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610
  • Z-0485-2022 · Dec 7, 2021 · Terminated
    GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600
  • Z-0488-2022 · Dec 7, 2021 · Terminated
    GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100
  • Z-0486-2022 · Dec 7, 2021 · Terminated
    GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100
  • Z-0484-2022 · Dec 7, 2021 · Terminated
    GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100
  • Z-0490-2022 · Dec 7, 2021 · Terminated
    GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100

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

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

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page