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Comprehensive® Reverse Shoulder Instrument 405809Recalls & reported problems

Biomet Orthopedics, LLC · Class 2

Data updated Oct 16, 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 00887868504600), received between Feb 14, 2022 and Feb 14, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (1 report).

6 other recalls cover devices cleared under the same FDA submission (K120121, K132239, K193373); 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

  • Fracture1

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.

  • MalfunctionFeb 14, 2022Fracture; Fracture

    IT WAS REPORTED THAT THE INSTRUMENT FRACTURED DURING THE PROCEDURE. THERE WAS NO REPORTED PATIENT INJURY AND ALL PIECES WERE RETRIEVED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13523137 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K120121, K132239, K193373. One submission often covers many models, so check the product and lot details in each record.

  • Z-1131-2021 · Jan 15, 2021 · Terminated
    Central Screw 6.5x25mm - Product Usage: used as a sterile screw that is intended for implantable shoulder prosthesis assembly and/or fixation.
  • Z-0619-2021 · Nov 25, 2020 · Terminated
    Comprehensive Reverse Shoulder System, Item numbers 115394, 115395, 115396, 115398, 180550, 180551, 180552, 180553, 180554, 180555, 180556, 180557, 180558, 180559, 180560, 1805
  • Z-0093-2021 · Sep 2, 2020 · Terminated
    Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper Adapter-Shoulder Prosthesis item: 010000589 - Product Usage: intended to serve as the foundation for t
  • Z-1615-2020 · Feb 25, 2020 · Terminated
    Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate With Taper Adapter-indicated for primary, fracture, or revision total shoulder replacement for the relief of pain a
  • Z-0972-2019 · Dec 21, 2018 · Terminated
    Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 010000589 Biomet Comprehensive Reverse Shoulder products are indicated for use i
  • Z-1208-2015 · Jan 7, 2015 · Terminated
    Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor, Part Number: 010000589 Lot: 527400

Other shoulder prosthesis, reverse configuration devices

All shoulder prosthesis, reverse configuration devices →

Sources and updates

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