--- title: "Scientia Vascular, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Scientia Vascular, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/scientia-vascular-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Scientia Vascular, Inc. recall records **3** reported ongoing 3 records in this archive. Latest source date Jan 16, 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 Jan 16, 2025 FDA device enforcement ### [Plato 17 Microcatheter REF PL17-160-090 To assist in delivery of therapeutic devices and embolization materials and infusion of diagnostic agents to the neuro and peripheral vas...](https://isitonrecall.com/recall/fda-device-z-1235-2025-plato-17-microcatheter-ref-pl17-160-090-to-assist-in-delivery-of-therapeutic-devices-and-embolizatio/) Due to manufacturing non-conformance that resulted in channels in the seal on the packaging pouch. As a result, this could potential create a breach in the sterile barrier. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the state of DE. [Official source for Plato 17 Microcatheter REF PL17-160-090 To assist in delivery of therapeutic devices and emboliza...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1235-2025%22) Jan 2, 2025 FDA device enforcement ### [Socrates 38 Aspiration Catheter 127 cm length REF SC038-127-001 The Socrates Aspiration System with a compatible suction pump is intended for use in the revascularization of pat...](https://isitonrecall.com/recall/fda-device-z-1234-2025-socrates-38-aspiration-catheter-127-cm-length-ref-sc038-127-001-the-socrates-aspiration-system-with/) Due to manufacturing non-conformance that resulted in channels in the seal on the packaging pouch. As a result, this could potential create a breach in the sterile barrier. Class II Reported ongoing Distribution: U..S. Nationwide distribution in the states of AL, AZ, FL, GA, HI, IL, IN, KS, MN, NC, NJ, NY, PA, SD, TX, VA, WI and WV. [Official source for Socrates 38 Aspiration Catheter 127 cm length REF SC038-127-001 The Socrates Aspiration System wi...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1234-2025%22) Feb 1, 2023 FDA device enforcement ### [Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090](https://isitonrecall.com/recall/fda-device-z-1249-2023-plato-17-microcatheter-straight-tip-pl17-160-000-45-degree-tip-pl17-160-045-90-degree-tip-pl17-160-0/) Microcatheters for embolic coil and diagnostic agent introduction to peripheral/neuro vasculature, due to manufacturing non-conformance, and due to flush, guidewire insertion and manipulation prior to placement, may have loose particles within catheter lume... Class II Reported ongoing Distribution: US Nationwide distribution in the states of IL, AL, FL, NC, WI, GA, SC, IN, KS, CA, OH, NY, NH, CO, MA, NV, UT, TX. [Official source for Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1249-2023%22) ## Reasons in these listed records - Due to manufacturing non-conformance that resulted in channels in the seal on the packaging pouch. As a result, this could potential create a breach in the sterile barrier. - Microcatheters for embolic coil and diagnostic agent introduction to peripheral/neuro vasculature, due to manufacturing non-conformance, and due to flush, guidewire insertion and manipulation prior to placement, may have loose particles within catheter lumens that may be intro... These examples come from this result page and are not a ranking of every recall reason. ## Checking Scientia Vascular, Inc. ### Is there a recall on scientia vascular, inc. right now? This archive contains 3 records, including 3 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 Scientia Vascular, Inc.](https://isitonrecall.com/check/?q=Scientia%20Vascular%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)