Lower riskMedical device recall · FDA · Published August 29, 2023
Limacorporate PRIMA TT Baseplates Recall: Risk of Loose Implant Due to Manufacturing Issue
Limacorporate recalls specific PRIMA TT Glenoid Monoblock baseplates with potential for loosening due to manufacturing defects. Affected models include D.25mm and D.28mm versions with various wedge angles. Consumers should check product codes and contact Limacorporate for details.
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.
Take action
Contact the company
📍Recalling firmLimacorporate S.p.AVia Nazionale 52, Di San Daniele · San Daniele Del Friuli, Italy
“Limacorporate PRIMA TT Baseplates Recall: Risk of Loose Implant Due to Manufacturing Issue.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57436-limacorporate-prima-tt-baseplates-recall-risk-of-loose-implant-due. Based on FDA recall #Z-0726-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0726-2024%22&limit=1).
The FDA announced on 2023-08-29 that Limacorporate S.p.A. is recalling PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates due to a manufacturing issue causing peripheral holes to be out of specification, which could lead to implant loosening or screw displacement.
How to tell if you have it
Brand: Limacorporate
Product: PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates
Product Code: BASEPLATE D.25MM REGULAR/1975.14.500, BASEPLATE D.28MM REGULAR/1975.14.800, BASEPLATE D.25MM FULL WEDGED 10-degrees/1975.14.510, BASEPLATE D.28MM FULL WEDGED 10-degrees/1975.14.810, BASEPLATE D.25MM FULL WEDGED 15-degrees/1975.14.615, BASEPLATE D.28MM FULL WEDGED 15-degrees/1975.14.815, BASEPLATE D.28MM FULL WEDGED 15-degrees X/1975.14.865, BASEPLATE D.25 MM FULL WEDGED 20-degrees/1975.14.620, BASEPLATE D.28 MM FULL WEDGED 20-degrees/1975.14.820, BASEPLATE D.28 MM FULL WEDGED 20-degrees X/1975.14.870
According to the FDA, the potential for baseplate peripheral holes to be out of specification due to a manufacturing issue could lead to loosening of the implant or the screw moving from its original position.
Context
GovInfoNow's records show Limacorporate S.p.A has had 8 other recalls on record since 2017-09-08. Other recent recalls include the Limacorporate PRIMA 2MM Eccentric Adaptor Recall (2025-05-19), the Limacorporate TEMA Elbow Prostheses Recall (2024-10-02), and the Limacorporate PHYSICA HPS Tibial Liner #6 H10 Recall (2023-10-27). Other recent recalls of similar products include the restor3d Veritas Standard Glenoid Baseplate Recall (2026-06-30), the Olympus HX-400U-30 Ligating Device Recall (2025-10-30), and the Howmedica SCORPIO C-DOME/PATELLA Implants Recall (2026-07-30).
How to tell if you have this one
Check if your PRIMA TT Glenoid Monoblock baseplate has a product code starting with 1975.14.500, 1975.14.800, or similar codes listed in the recall. The baseplate may have a diameter of 25mm or 28mm with specific wedge angles.
Brand
Limacorporate
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Code
Look for the product code on your baseplate, which starts with 1975.14 and includes a unique number like 08033390244824.
Contact Limacorporate
Reach out to Limacorporate directly for confirmation of your product and instructions on next steps.
Where it went and when
Where it was distributed
Distributed in 6 states.
Listed by the agency
Not listed
FDA distribution: “US: IL, MO, CA, IN, MI, OK” States read from FDA’s own wording; “not listed” means the notice does not name it.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0726-2024 (August 29, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0726-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.