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Comprehensive® Shoulder System 113610Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

All models of Comprehensive Shoulder System (68)

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 00887868267604), received between Dec 12, 2022 and Dec 12, 2022 — classified as 1 injury.

7 other recalls cover devices cleared under the same FDA submission (K060692, K193038); 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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Failure of Implant1
  • Pain1
  • Synovitis1

Recent adverse event reports

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

  • InjuryDec 12, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A PATIENT IS TO UNDERGO A REVISION SIX(6) YEARS POST IMPLANTATION DUE DISASSOCIATION AND PAIN. HOWEVER, NO REVISION PROCEDURE HAS BEEN REPORTED TO DATE. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED

    Patient problems: Failure of Implant; Pain; Synovitis

    MAUDE report 15959371 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K060692, K193038. One submission often covers many models, so check the product and lot details in each record.

  • Z-1403-2025 · Mar 3, 2025 · Open, Classified
    Comprehensive Shoulder Stem, Comprehensive Micro Stem, Comprehensive Mini Stem; uncemented shoulder prosthesis, Model Nos. 113605, 113606, 113607, 113627
  • Z-1543-2020 · Feb 17, 2020 · Terminated
    Comprehensive Shoulder System Mini Humeral Stem 9mm,, Model No. 113629 - Product Usage: The intended use of the comprehensive humeral stem mini is to act as the humeral component o
  • Z-0591-2019 · Oct 10, 2018 · Terminated
    Comprehensive Mini Stem, Item No. 113631:
  • Z-0980-2018 · Dec 8, 2017 · Terminated
    Humeral Stem 55mm(Size 13) Product Usage: Intended for primary and revision total shoulder arthroplasty as well as hemi-arthroplasty
  • Z-0979-2018 · Dec 8, 2017 · Terminated
    Humeral Stem 83mm(Size 17) Product Usage: Intended for primary and revision total shoulder arthroplasty as well as hemi-arthroplasty
  • Z-0299-2018 · Jun 5, 2017 · Terminated
    COMP PRIMARY STEM 8MM MINI, model # 113628
  • Z-1755-2015 · Apr 16, 2015 · Terminated
    Comprehensive Shoulder System, 4 mm, 122 mm long, Primary Shoulder Stem, Ti-6Al-4V, Standard Length Porous Plasma. Shoulder joint replacement components include humeral stems, hum

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