--- title: "Preat Corp Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Preat Corp recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/preat-corp/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Preat Corp recall records **11** reported ongoing 11 records in this archive. Latest source date Jun 25, 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 Jun 25, 2025 FDA device enforcement ### [NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662](https://isitonrecall.com/recall/fda-device-z-2514-2025-nobelbiocare-tri-lobe-compatible-wp-x-6-0mm-engaging-titanium-base-ref-9000662/) Engaging titanium base was manufactured 180 degrees around the post from where it should be located in relation to the connection geometry; if the flat is on the wrong side of the post, the crown will not fit onto the abutment in the correct orientation, re... Class II Reported ongoing Distribution: US Nationwide distribution in the states of NY, FL, PA, CA, OH. [Official source for NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2514-2025%22) Jun 24, 2025 FDA device enforcement ### [Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only](https://isitonrecall.com/recall/fda-device-z-2107-2025-preat-astra-ev-compatible-4-2mm-digital-analog-ref-9006603-single-and-9006603-10-10-pack-rx-only/) Due to manufacturing error, digital analog rotational feature is 180 degrees off. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, CA, FL, GA, KY, MD, MN, NY, OK, PA. [Official source for Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2107-2025%22) Apr 2, 2025 FDA device enforcement ### [Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxilla...](https://isitonrecall.com/recall/fda-device-z-1987-2025-biomet-3i-certain-compatible-4-1-mm-milled-ti-abutment-ref-9001767-f-preat-milled-abutments-are-inte/) Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of AZ, CA, GA, MO, NJ, NY, OH, PA, RI, TN,TX, and WA. [Official source for Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are i...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1987-2025%22) Jun 25, 2024 FDA device enforcement ### [Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann Tissue-Level-compatible WN Digital Analog, REF 9001303 ...](https://isitonrecall.com/recall/fda-device-z-2687-2024-multiple-digital-analog-products-labeled-as-nobelbiocare-tri-lobe-compatible-6-0mm-digital-analog-re/) Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of AK, AZ, FL, GA, IL, LA, MD, MI, MN, NY, OH, OK, OR, PA, RI, TX, UT, and WA [Official source for Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analo...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2687-2024%22) Apr 10, 2024 FDA device enforcement ### [9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.](https://isitonrecall.com/recall/fda-device-z-2318-2024-9006767-astra-ev-4-8mm-milled-titanium-abutment-milled-abutments-are-too-be-used-in-conjunction-with/) Due to incorrect milled titanium abutment being packaged and labeled. Class II Reported ongoing Distribution: U.S.: CA, MO, and NV. O.U.S.: None [Official source for 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction w...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2318-2024%22) Feb 9, 2024 FDA device enforcement ### [Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967](https://isitonrecall.com/recall/fda-device-z-1321-2024-preat-nobel-active-conical-compatible-rp-titanium-blank-ref-9000967/) Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of AZ, OH and PA. [Official source for Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1321-2024%22) Jul 18, 2023 FDA device enforcement ### [Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental](https://isitonrecall.com/recall/fda-device-z-0152-2024-preat-ref-9007121-neodent-gm-x-2mm-healing-abutment-rx-only-non-sterile-single-use-only-dental/) The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage Class II Reported ongoing Distribution: US: FL, CA, OR, TX, OH, CA, SC, OR, NJ, SC, OUS: None [Official source for Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0152-2024%22) Jul 18, 2023 FDA device enforcement ### [Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental](https://isitonrecall.com/recall/fda-device-z-0153-2024-preat-ref-9007123-neodent-gm-x-4mm-healing-abutment-rx-only-non-sterile-single-use-only-dental/) The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage Class II Reported ongoing Distribution: US: FL, CA, OR, TX, OH, CA, SC, OR, NJ, SC, OUS: None [Official source for Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0153-2024%22) Jul 18, 2023 FDA device enforcement ### [Preat REF 9007124, Neodent GM x 4mm Healing Abutment (Wide), Rx Only, Non-Sterile, Single Use Only. Dental](https://isitonrecall.com/recall/fda-device-z-0154-2024-preat-ref-9007124-neodent-gm-x-4mm-healing-abutment-wide-rx-only-non-sterile-single-use-only-dental/) The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage Class II Reported ongoing Distribution: US: FL, CA, OR, TX, OH, CA, SC, OR, NJ, SC, OUS: None [Official source for Preat REF 9007124, Neodent GM x 4mm Healing Abutment (Wide), Rx Only, Non-Sterile, Single Use Onl...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0154-2024%22) Feb 21, 2023 FDA device enforcement ### [Neodent GM X 6mm Engaging Titanium Base, REF: 9007162](https://isitonrecall.com/recall/fda-device-z-1285-2023-neodent-gm-x-6mm-engaging-titanium-base-ref-9007162/) Engaging titanium base contains a dimensional condition that allows vertical movement of the titanium base after the prosthetic screw is torqued to the recommended value, which if undetected and installed on the implant, may lead to abutment/screw fracture,... Class II Reported ongoing Distribution: US Nationwide distribution in the states of TX, OR, UT, NY. [Official source for Neodent GM X 6mm Engaging Titanium Base, REF: 9007162](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1285-2023%22) Feb 1, 2023 FDA device enforcement ### [PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.](https://isitonrecall.com/recall/fda-device-z-1226-2023-preat-nobil-grip-product-numbers-0102000-and-01202000-3-3-pack-5-ml-vials-packaged-in-pouches-dental/) Product is labeled with an incorrect expiration date. Class III Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, MS, NC, NJ, NY, OK, PA, SC, SD, TN, TX, UT,... [Official source for PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1226-2023%22) ## Reasons in these listed records - Engaging titanium base was manufactured 180 degrees around the post from where it should be located in relation to the connection geometry; if the flat is on the wrong side of the post, the crown will not fit onto the abutment in the correct orientation, resulting in restorati... - Due to manufacturing error, digital analog rotational feature is 180 degrees off. - Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant. - Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations. These examples come from this result page and are not a ranking of every recall reason. ## Checking Preat Corp ### Is there a recall on preat corp right now? This archive contains 11 records, including 11 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 Preat Corp](https://isitonrecall.com/check/?q=Preat%20Corp) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)