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PRIMA TT Glenoid 1975.14.820Recalls & reported problems

Limacorporate SPA · PRIMA TT Glenoid - Modular Reverse TT Baseplate Dia. 28 mm; Full Wedge 20° · Class 2 · Implant

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

  1. Aug 29, 2023Open, Classified

    Potential for baseplate peripheral holes to be out of specification due to a manufacturing issue, which could lead to loosening of the implant, or the screw moving from its original position.

    Z-0726-2024 · Root cause: Device Design · FDA record ↗

Other Shoulder Prosthesis, Reverse Configuration devices

All Shoulder Prosthesis, Reverse Configuration devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.