--- title: "Cook Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Cook 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/cook-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Cook Inc. recall records **1** reported ongoing 5 records in this archive. Latest source date Nov 12, 2021. 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 Nov 12, 2021 FDA device enforcement ### [Flexor Check-Flo Introducer Ansel Modification Model Number: KCFW-6.0-18/38-45-RB-ANL0-HC Order Number/GPN: G44154 Intended to introduce therapeutic or diagnostic devices into t...](https://isitonrecall.com/recall/fda-device-z-0387-2022-flexor-check-flo-introducer-ansel-modification-model-number-kcfw-6-0-18-38-45-rb-anl0-hc-order-numbe/) Flexor Check-Flo Introducer Ansel Modification mislabeled. Products packaged with a label stating 6FR may contain a 7FR device and vice versa Class II Reported terminated Distribution: AL, AZ, CA, FL, GA, KS, MI, MO, MN, NC, NY, OK, TX Foreign: BE, CH, DE, ES, FR, GB,GU, IT, ZA [Official source for Flexor Check-Flo Introducer Ansel Modification Model Number: KCFW-6.0-18/38-45-RB-ANL0-HC Order N...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0387-2022%22) Nov 12, 2021 FDA device enforcement ### [Flexor Check-Flo Introducer Ansel Modification Model Number: KCFW-7.0-18/38-45-RB-ANL0-HC Order Number/GPN: G44155 Intended to introduce therapeutic or diagnostic devices into t...](https://isitonrecall.com/recall/fda-device-z-0388-2022-flexor-check-flo-introducer-ansel-modification-model-number-kcfw-7-0-18-38-45-rb-anl0-hc-order-numbe/) Flexor Check-Flo Introducer Ansel Modification mislabeled. Products packaged with a label stating 6FR may contain a 7FR device and vice versa Class II Reported terminated Distribution: AL, AZ, CA, FL, GA, KS, MI, MO, MN, NC, NY, OK, TX Foreign: BE, CH, DE, ES, FR, GB,GU, IT, ZA [Official source for Flexor Check-Flo Introducer Ansel Modification Model Number: KCFW-7.0-18/38-45-RB-ANL0-HC Order N...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0388-2022%22) Oct 13, 2021 FDA device enforcement ### [Skinny Needle with Chiba Tip. RPN 090010, 090010-ET; GPN G14254, G15290. Rigid needle available with EchoTip to provide enhanced visualization of needle tip when used with ultra...](https://isitonrecall.com/recall/fda-device-z-0414-2022-skinny-needle-with-chiba-tip-rpn-090010-090010-et-gpn-g14254-g15290-rigid-needle-available-with-echo/) Specific lots may contain black debris on the exterior of the inner stylet and/or on the interior of the outer cannula. Local inflammatory reactions may occur if an affected product is used. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of AL, CA, IN, LA, MS, MT, NC, NY, OR, PA, WA and the countries of France, Italy, and Mexico. [Official source for Skinny Needle with Chiba Tip. RPN 090010, 090010-ET; GPN G14254, G15290. Rigid needle available w...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0414-2022%22) Oct 8, 2021 FDA device enforcement ### [Transseptal Needle, Trocar. RPN TSNC-18-71.0, TSNC-19-56.0. GPN G02364, G02365. Product consists of a transseptal needle and obturator.](https://isitonrecall.com/recall/fda-device-z-0222-2022-transseptal-needle-trocar-rpn-tsnc-18-71-0-tsnc-19-56-0-gpn-g02364-g02365-product-consists-of-a-tran/) Transseptal needles may contain rust on the interior and/or exterior of the needle, which may not be detected by the user. Potential adverse events if an affected product is used ranges from increased procedural time to inflammatory reactions, which at thei... Class II Reported terminated Distribution: Domestic distribution nationwide. Foreign distribution worldwide. [Official source for Transseptal Needle, Trocar. RPN TSNC-18-71.0, TSNC-19-56.0. GPN G02364, G02365. Product consists ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0222-2022%22) Oct 8, 2021 FDA device enforcement ### [Transseptal Needle with Catheter. RPN TSN-17-75.0-ENDRYS. GPN G19261. Coaxial set consisting of an outer catheter, curved-tip metal cannula, and a tapered-tip inner needle](https://isitonrecall.com/recall/fda-device-z-0223-2022-transseptal-needle-with-catheter-rpn-tsn-17-75-0-endrys-gpn-g19261-coaxial-set-consisting-of-an-oute/) Transseptal needles may contain rust on the interior and/or exterior of the needle, which may not be detected by the user. Potential adverse events if an affected product is used ranges from increased procedural time to inflammatory reactions, which at thei... Class II Reported terminated Distribution: Domestic distribution nationwide. Foreign distribution worldwide. [Official source for Transseptal Needle with Catheter. RPN TSN-17-75.0-ENDRYS. GPN G19261. Coaxial set consisting of a...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0223-2022%22) ## Reasons in these listed records - Flexor Check-Flo Introducer Ansel Modification mislabeled. Products packaged with a label stating 6FR may contain a 7FR device and vice versa - Specific lots may contain black debris on the exterior of the inner stylet and/or on the interior of the outer cannula. Local inflammatory reactions may occur if an affected product is used. - Transseptal needles may contain rust on the interior and/or exterior of the needle, which may not be detected by the user. Potential adverse events if an affected product is used ranges from increased procedural time to inflammatory reactions, which at their most severe includ... These examples come from this result page and are not a ranking of every recall reason. ## Checking Cook Inc. ### Is there a recall on cook inc. right now? This archive contains 5 records, including 1 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 Cook Inc.](https://isitonrecall.com/check/?q=Cook%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)