--- title: "Limacorporate S.p.A Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Limacorporate S.p.A recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/limacorporate-s-p-a/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Limacorporate S.p.A recall records **9** reported ongoing 11 records in this archive. Latest source date May 19, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status May 19, 2025 FDA device enforcement ### [PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW REF: 1367.15.702, Sterile](https://isitonrecall.com/recall/fda-device-z-2024-2025-prima-2mm-eccentrical-adaptor-with-screw-ref-1367-15-702-sterile/) There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of VA, FL, SC, MS, NY, TX and the countries of Italy, Poland, France. [Official source for PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW REF: 1367.15.702, Sterile](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2024-2025%22) May 19, 2025 FDA device enforcement ### [PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile](https://isitonrecall.com/recall/fda-device-z-2025-2025-prima-4mm-eccentrical-adaptor-with-screw-ref-1367-15-704-sterile/) There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of VA, FL, SC, MS, NY, TX and the countries of Italy, Poland, France. [Official source for PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2025-2025%22) Oct 2, 2024 FDA device enforcement ### [TEMA Elbow - Axle Small REF 1590.15.010 TEMA Elbow - Axle Large REF 1590.15.020 TEMA Elbow System is a cemented total elbow prosthesis.](https://isitonrecall.com/recall/fda-device-z-0744-2025-tema-elbow-axle-small-ref-1590-15-010-tema-elbow-axle-large-ref-1590-15-020-tema-elbow-system-is-a-c/) Due to a potential difference in mechanical behavior between the implanted device and tool(s) used during revision surgery. Class II Reported ongoing Distribution: U.S: FL and TX O.U.S.: N/A [Official source for TEMA Elbow - Axle Small REF 1590.15.010 TEMA Elbow - Axle Large REF 1590.15.020 TEMA Elbow System...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0744-2025%22) Oct 27, 2023 FDA device enforcement ### [PHYSICA HPS Tibial Liner #6 H10 REF 6539.54.610](https://isitonrecall.com/recall/fda-device-z-0524-2024-physica-hps-tibial-liner-6-h10-ref-6539-54-610/) Due to incorrect product labeling Class II Reported ongoing Distribution: U.S Distribution: AZ, CA, IL, LA, and NY [Official source for PHYSICA HPS Tibial Liner #6 H10 REF 6539.54.610](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0524-2024%22) Aug 29, 2023 FDA device enforcement ### [PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code: BASEPLATE D.25MM REGULAR/1975.14.500, BASEPLATE D.28MM REGULAR/1975.14.800, BASEPLATE D.25MM ...](https://isitonrecall.com/recall/fda-device-z-0726-2024-prima-tt-glenoid-monoblock-modular-reverse-tt-baseplates-description-product-code-baseplate-d-25mm-r/) 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. Class II Reported ongoing Distribution: US: IL, MO, CA, IN, MI, OK [Official source for PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code: BASEPLATE D.2...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0726-2024%22) May 30, 2023 FDA device enforcement ### [REF 1975.14.500, Prima TT Genoid Monoblock Reverse TT Baseplate, STERILE R](https://isitonrecall.com/recall/fda-device-z-2009-2023-ref-1975-14-500-prima-tt-genoid-monoblock-reverse-tt-baseplate-sterile-r/) Due to manufacturing issue, their is a potential for peripheral holes to be out of specification. Class II Reported ongoing Distribution: US Nationwide distribution in the states of MI, IL, ND, MO, OK. [Official source for REF 1975.14.500, Prima TT Genoid Monoblock Reverse TT Baseplate, STERILE R](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2009-2023%22) May 30, 2023 FDA device enforcement ### [REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R](https://isitonrecall.com/recall/fda-device-z-2010-2023-ref-1975-14-800-prima-tt-genoid-modular-reverse-tt-baseplate-sterile-r/) Due to manufacturing issue, their is a potential for peripheral holes to be out of specification. Class II Reported ongoing Distribution: US Nationwide distribution in the states of MI, IL, ND, MO, OK. [Official source for REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2010-2023%22) Feb 21, 2023 FDA device enforcement ### [SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210](https://isitonrecall.com/recall/fda-device-z-1317-2023-smr-tt-hybrid-glenoid-std-peg-s-ref-1379-59-210/) Shoulder glenoid fossa prosthesis was manufactured without tantalum markers so in the absence of the markers, on already implanted devices, a correct radiographic assessment of the hybrid glenoid position can be performed by the evaluation of the joint spac... Class II Reported ongoing Distribution: US: MO [Official source for SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1317-2023%22) Jan 25, 2023 FDA device enforcement ### [TEMA Axle Small, REF 1590.15.010 (additional information is pending receipt of the firm's product label/labeling)](https://isitonrecall.com/recall/fda-device-z-1261-2023-tema-axle-small-ref-1590-15-010-additional-information-is-pending-receipt-of-the-firm-s-product-labe/) Due to the incorrect component, that is not cleared to be marketed in the U.S., being included in its elbow prosthesis. Class II Reported ongoing Distribution: U.S. Distribution to: TX [Official source for TEMA Axle Small, REF 1590.15.010 (additional information is pending receipt of the firm's product...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1261-2023%22) Oct 1, 2021 FDA device enforcement ### [REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERILE R, 2100099, UDI: (01)08033390018852](https://isitonrecall.com/recall/fda-device-z-0159-2022-ref-8420-15-020-bone-screw-vite-ti6ai4v-self-tapping-autofilettante-dia-6-5mm-h-25mm-sterile-r-21000/) There is a potential that the length of bone screws identified on labeling may not correspond to the actual length of the screw included. Class II Reported terminated Distribution: Worldwide distribution - US Nationwide distribution in the states of CA, FL, MO, KS, CO, TX, KS, IL, PA, NY, NC, MI, MA, OK and the countries of Austria, Croatia, Germany, Irela... [Official source for REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERI...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0159-2022%22) Oct 1, 2021 FDA device enforcement ### [REF 8420.15.010, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=20mm, STERILE R, 2100099, UDI: (01)08033390018845](https://isitonrecall.com/recall/fda-device-z-0160-2022-ref-8420-15-010-bone-screw-vite-ti6ai4v-self-tapping-autofilettante-dia-6-5mm-h-20mm-sterile-r-21000/) There is a potential that the length of bone screws identified on labeling may not correspond to the actual length of the screw included. Class II Reported terminated Distribution: Worldwide distribution - US Nationwide distribution in the states of CA, FL, MO, KS, CO, TX, KS, IL, PA, NY, NC, MI, MA, OK and the countries of Austria, Croatia, Germany, Irela... [Official source for REF 8420.15.010, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=20mm, STERI...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0160-2022%22) ## Reasons in these listed records - There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing. - Due to a potential difference in mechanical behavior between the implanted device and tool(s) used during revision surgery. - Due to incorrect product labeling - 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. These examples come from this result page and are not a ranking of every recall reason. ## Checking Limacorporate S.p.A ### Is there a recall on limacorporate s.p.a right now? This archive contains 11 records, including 9 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Limacorporate S.p.A](https://isitonrecall.com/check/?q=Limacorporate%20S.p.A) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)