PRIMA TT Glenoid 1975.14.615Recalls & reported problems
Limacorporate SPA · PRIMA TT Glenoid - Modular Reverse TT Baseplate Dia. 25 mm; Full Wedge 15° · Class 2 · Implant
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08033390244848), received between Aug 1, 2025 and Aug 1, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (1 report).
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.
Reports received per month
Recalls naming this device
- 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 ↗
Most reported problems
Device problems
- Patient Device Interaction Problem1
Patient problems
- Implant Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 1, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
SHOULDER REVISION SURGERY DUE TO LOOSENING OF THE GLENOID COMPONENT PERFORMED ON (B)(6) 2025. THE ORIGINAL SURGERY TOOK PLACE ON (B)(6), FEW WEEKS LATER, THE PATIENT SHOWED UP IN CLINIC COMPLAINING OF PAIN. SHE DIDN'T DESCRIBE AN INCIDENT. THE X-RAYS REVEALED LOOSE GLENOID COMPONENT. ON (B)(6), THE SURGEON REVISED THE PATIENT WITH BONE GRAFTING AND REPLACING THE GLENOID. SIGNIFICANT BONE LOSS WAS NOTED. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION. THE BASEPLATE INVOLVED IN THE COMPLAINT IS THE FOLLOWING: BASEPLATE D.25MM FULL WEDGE15°, PRODUCT CODE 1975.14.615, LOT N. 2435904, STER. (B)(4). THE PATIENT IS FEMALE, BORN IN 1945. THE EVENT HAPPENED IN THE UNITED STATES.
Patient problems: Implant Pain
MAUDE report 22687144 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.