Lower riskMedical device recall · FDA · Published May 30, 2023
Limacorporate S.p.A Prima TT Genoid Modular Baseplate Recall: Peripheral Holes May Be Out
Limacorporate S.p.A recalls Prima TT Genoid Modular Reverse TT Baseplate (Sterile R) due to potential peripheral holes being out of specification. All lots are affected.
Due to manufacturing issue, their is a potential for peripheral holes to be out of specification.
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Contact the company
📍Recalling firmLimacorporate S.p.AVia Nazionale 52, Di San Daniele · San Daniele Del Friuli, Italy
✎ GovInfoNow plain-language explainer
Limacorporate S.p.A is recalling all units of their Prima TT Genoid Modular Reverse TT Baseplate (Sterile R) because manufacturing issues may cause peripheral holes to be out of specification. This could affect the product's proper function or safety. Read more at govinfonow.com/recall/57940-limacorporate-s-p-a-prima-tt-genoid-modular-baseplate-recall.
“Limacorporate S.p.A Prima TT Genoid Modular Baseplate Recall: Peripheral Holes May Be Out.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57940-limacorporate-s-p-a-prima-tt-genoid-modular-baseplate-recall. Based on FDA recall #Z-2010-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2010-2023%22&limit=1).
The FDA announced on May 30, 2023, that Limacorporate S.p.A. is recalling REF 1975.14.800 Prima TT Genoid Modular Reverse TT Baseplate, Sterile R due to a manufacturing issue where peripheral holes may be out of specification.
How to tell if you have it
Brand: Limacorpor: S.p.A
Product: REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R
UDI-DI: 08033390244893
Lots: All Lots
Quantity: 13 units
Distribution: US Nationwide in MI, IL, ND, MO, OK
The hazard
According to the FDA, there is a potential for peripheral holes to be out of specification due to a manufacturing issue.
Context
GovInfoNow's records show Limacorporate S.p.A has had 8 other recalls on record since September 8, 2017. Other recent recalls include the May 19, 2025 PRIMA 2MM Eccentric Adaptor Recall and the October 2, 2024 TEMA Elbow Prostheses Recall. Similar product recalls in this sector include the October 30, 2025 Olympus HX-400U-30 Ligating Device Recall, the June 30, 2026 restor3d Veritas Standard Glenoid Baseplate Recall, and the July 30, 2026 Howmedica SCORPIO Patella Implants Recall.
How to tell if you have this one
Check for the product name 'Prima TT Genoid Modular Reverse TT Baseplate, Sterile R' and the UDI-DI code 08033390244893. All lots of this product are affected.
Brand
Limacorpor: S.p.A
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution in the states of MI, IL, ND, MO, OK.
Recall number
Product, codes & lots
Z-2009-2023
REF 1975.14.500, Prima TT Genoid Monoblock Reverse TT Baseplate, STERILE R; UDI-DI: 08033390244824; All Lots
Z-2010-2023
REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R; UDI-DI: 08033390244893; All Lots
Based on the official FDA remedy
What to do — step by step
Check Product Details
Identify the product name and UDI-DI code to confirm if your item is recalled.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 5 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of MI, IL, ND, MO, OK.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Illinois, Michigan, Missouri, North Dakota, Oklahoma.
Recall timeline
FDA published this recall 36 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-2010-2023 (May 30, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2010-2023 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.