PRIMA TT Glenoid 1975.15.594Recalls & reported problems
Limacorporate SPA · PRIMA TT Glenoid - 4x Locking Caps · Class 2
All models of PRIMA TT Glenoid (16)
Data updated Oct 18, 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 08033390239714), received between Dec 2, 2025 and Dec 2, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Product Quality Problem” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Product Quality Problem1
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.
MalfunctionDec 2, 2025Product Quality Problem; Product Quality Problem
DURING SURGERY, TWO SEPARATE PACKAGES OF LOCKING CAPS (PRODUCT CODE: 1975.15.594, LOT: 2434865 - STER: 2500040) WERE OPENED, BUT THE CAPS COULD NOT BE APPLIED DUE TO FAILURE OF THE ANGLE-STABLE LOCKIAG MECHANISM. THAT ISSUE PREVENTED PROPER FIXATION. THE PROCEDURE COULD NOT BE CARRIED OUT AS PLANNED BECAUSE THE ANGULAR-STABLE CAPS COULD NOT BE IMPLANTED DUE TO THE ISSUE ON CAP CLOSURE. THIS RESULTED IN A DELAY OF APPROXIMATELY 15-20 MINUTES. THE DEVICES HAVE BEEN DISCARDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23692503 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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