COMPREHENSIVE SHOULDER SYSTEM 110004319Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00880304539297), received between Oct 17, 2019 and Oct 17, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

4 other recalls cover devices cleared under the same FDA submission (K060694); 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

Recent adverse event reports

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

• MalfunctionOct 17, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT PATIENT UNDERWENT SHOULDER PROCEDURE (B)(6) 2019 AND DURING THE REMOVAL OF THE DRILL GUIDE THE SMALL SPRING MECHANISM FELL APART INTO FOUR PIECES INCLUDING THE CENTRAL SHAFT, SPRING, SMALL SCREW AND THE HAND PIECE. NO FURTHER INFORMATION AVAILABLE AT THE TIME OF THIS REPORTING.

  Patient problems: No Information

  MAUDE report 9203594 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K060694. One submission often covers many models, so check the product and lot details in each record.

• Z-2216-2017 · Apr 26, 2017 · Terminated
  Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System, The product is placed into an AlOx coated PET pouch and vacuum sealed with an Argon flush. The vacuum seale
• Z-1859-2017 · Feb 17, 2017 · Terminated
  various polyethylene implants Extremities, Shoulders and Elbows BioModular Shoulder System; Comprehensive Shoulder System; Comprehensive Reverse Shoulder System Product Usage: Sh
• Z-1658-2008 · Mar 13, 2008 · Terminated
  Biomet Hybrid Glenoid Boss Cutter; item 406150. - Surgical instrument used to prepare the natural shoulder glenoid surface for implanting a Hybrid Glenoid component. This instrume
• Z-0660-2013 · Dec 6, 0012 · Terminated
  PT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct Sterile R Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented