PRIMA TT Glenoid 9019.74.140Recalls & reported problems
Limacorporate SPA · PRIMA TT Glenoid - Glenosphere/Baseplate Extractor · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 08033390241069), received between Jan 30, 2026 and Sep 21, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Mechanical Problem” (3 reports).
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Mechanical Problem3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 21, 2026Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50840364 ↗MalfunctionSep 21, 2026Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50839855 ↗MalfunctionJan 30, 2026Mechanical Problem
DURING SURGERY ON (B)(6) 2025 THE THREAD OF THE GLENOSPHERE EXTRACTOR INSTRUMENT (PRODUCT CODE: 9019.74.140; LOT NUMBER: UNKNOWN) DID NOT ENGAGE WITH THE GLENOSPHERE (PRODUCT CODE: 1974.54.440; LOT NUMBER: 2424139) AND THEREFORE COULD NOT BE USED TO EXTRACT THE GLENOSPHERE. THE SURGEON REMOVED THE GLENOSPHERE BY USING A HOOK TO TAP IT OUT AND THEN IMPLANTED A NEW GLENOSPHERE TO COMPLETE THE PROCEDURE. THE SURGICAL TIME WAS PROLONGED BY APPROXIMATELY 15 MINUTES DUE TO THIS ISSUE. EVENT OCCURRED IN SWITZERLAND.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24222954 ↗
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- DJO SURGICAL 508-32-103Encore Medical, L.P. · shoulder prosthesis, reverse configuration421 reports
- DJO SURGICAL 509-00-036Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall259 reports
- DJO SURGICAL 508-32-104Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall203 reports
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- DJO SURGICAL 508-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration122 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.