--- title: "Oscor Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Oscor 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/oscor-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Oscor Inc. recall records **3** reported ongoing 4 records in this archive. Latest source date Jun 10, 2026. 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 10, 2026 FDA device enforcement ### [Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F 13cm and 25cm. heart pump and accessories.](https://isitonrecall.com/recall/fda-device-z-2678-2026-abiomed-ref-0052-3025-introducer-kit-for-impella-hemostatic-peel-away-introducer-system-with-infusio/) Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region. Class I Reported ongoing Distribution: Distribution in the US state of MA [Official source for Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with In...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2678-2026%22) Jun 10, 2026 FDA device enforcement ### [Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F, 23F. heart pump and accessories.](https://isitonrecall.com/recall/fda-device-z-2679-2026-abiomed-ref-0052-3021-introducer-kit-for-impella-hemostatic-peel-away-introducer-system-with-infusio/) Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region. Class I Reported ongoing Distribution: Distribution in the US state of MA [Official source for Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel Away Introducer System with In...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2679-2026%22) Jun 10, 2026 FDA device enforcement ### [Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 23F. heart pump and accessories.](https://isitonrecall.com/recall/fda-device-z-2680-2026-abiomed-ref-0052-3006-introducer-kit-for-impella-hemostatic-peel-away-introducer-system-with-infusio/) Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region. Class I Reported ongoing Distribution: Distribution in the US state of MA [Official source for Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel Away Introducer System with In...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2680-2026%22) Dec 22, 2021 FDA device enforcement ### [Destino Twist 14F (also branded as Guidestar 14F)](https://isitonrecall.com/recall/fda-device-z-0646-2022-destino-twist-14f-also-branded-as-guidestar-14f/) There is potential for separation between the threaded hub and threaded cap at the proximal end of the device. Class II Reported completed Distribution: Distribution to TN and PA in USA OUS distribution to Czech Republic [Official source for Destino Twist 14F (also branded as Guidestar 14F)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0646-2022%22) ## Reasons in these listed records - Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region. - There is potential for separation between the threaded hub and threaded cap at the proximal end of the device. These examples come from this result page and are not a ranking of every recall reason. ## Checking Oscor Inc. ### Is there a recall on oscor inc. right now? This archive contains 4 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 Oscor Inc.](https://isitonrecall.com/check/?q=Oscor%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)