--- title: "TELEFLEX MEDICAL INC Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search TELEFLEX MEDICAL 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/teleflex-medical-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # TELEFLEX MEDICAL INC recall records **2** reported ongoing 9 records in this archive. Latest source date Apr 11, 2022. 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 Apr 11, 2022 FDA device enforcement ### [(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732, non-sterile; (3) Gibeck Humid-Vent Filter Compact S with Smooth-Flo/...](https://isitonrecall.com/recall/fda-device-z-1126-2022-1-gibeck-humid-vent-2s-flex-dc-product-17731-sterile-2-gibeck-humid-vent-2s-flex-dc-product-17732-n/) Reports received of torn corrugated breathing tubes. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NV, NY, OH, PA, ... [Official source for (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Prod...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1126-2022%22) Apr 11, 2022 FDA device enforcement ### [(1) Teleflex Flex tube, Product #20011, sterile; (2) Teleflex Smooth-Flo Flex with Double Swivel, Product #22511, sterile; (3) Teleflex Smooth-Flo Flex with Double Swivel, Produ...](https://isitonrecall.com/recall/fda-device-z-1127-2022-1-teleflex-flex-tube-product-20011-sterile-2-teleflex-smooth-flo-flex-with-double-swivel-product-22/) Reports received of torn corrugated breathing tubes. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NV, NY, OH, PA, ... [Official source for (1) Teleflex Flex tube, Product #20011, sterile; (2) Teleflex Smooth-Flo Flex with Double Swivel,...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1127-2022%22) Jan 11, 2022 FDA device enforcement ### [Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, containing components: PT-12709-CA, PT-12709-C, The Arrow-Trerotola Percutaneous Thromb...](https://isitonrecall.com/recall/fda-device-z-0623-2022-arrow-trerotola-over-the-wire-ptd-kit-percutaneous-thrombolytic-device-ref-pt-12709-wc-containing-co/) The firm received reports indicating PTD tip separation during use. Class I Reported terminated Distribution: Worldwide distribution: US Nationwide and the countries of AU, BE, CA, CL, CZ, DE, ES, FR, GB, IL, IT, KR, KW, NL, PA, PH, PT, SA, TR. [Official source for Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, contain...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0623-2022%22) Jan 11, 2022 FDA device enforcement ### [Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC containing components: PT-65709-C, PT-03009, PT-65709-HFS The Arrow-Trerotola Percutan...](https://isitonrecall.com/recall/fda-device-z-0624-2022-arrow-trerotola-over-the-wire-ptd-kit-percutaneous-thrombolytic-device-ref-pt-65709-hfwc-containing/) The firm received reports indicating PTD tip separation during use. Class I Reported terminated Distribution: Worldwide distribution: US Nationwide and the countries of AU, BE, CA, CL, CZ, DE, ES, FR, GB, IL, IT, KR, KW, NL, PA, PH, PT, SA, TR. [Official source for Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC contai...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0624-2022%22) Jan 11, 2022 FDA device enforcement ### [Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-C The Arrow-Trerotola Percutaneous Thrombolytic Device (PT...](https://isitonrecall.com/recall/fda-device-z-0625-2022-arrow-trerotola-over-the-wire-ptd-kit-percutaneous-thrombolytic-device-ref-pt-65709-w-containing-com/) The firm received reports indicating PTD tip separation during use. Class I Reported terminated Distribution: Worldwide distribution: US Nationwide and the countries of AU, BE, CA, CL, CZ, DE, ES, FR, GB, IL, IT, KR, KW, NL, PA, PH, PT, SA, TR. [Official source for Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containin...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0625-2022%22) Jan 11, 2022 FDA device enforcement ### [Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-WC containing components: PT-65709-C, PT-03009, PT-65709-HS The Arrow-Trerotola Percutaneou...](https://isitonrecall.com/recall/fda-device-z-0626-2022-arrow-trerotola-over-the-wire-ptd-kit-percutaneous-thrombolytic-device-ref-pt-65709-wc-containing-co/) The firm received reports indicating PTD tip separation during use. Class I Reported terminated Distribution: Worldwide distribution: US Nationwide and the countries of AU, BE, CA, CL, CZ, DE, ES, FR, GB, IL, IT, KR, KW, NL, PA, PH, PT, SA, TR. [Official source for Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-WC containi...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0626-2022%22) Jan 11, 2022 FDA device enforcement ### [Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), PT-45509 containing components: PT-45509-S6, PT-45509-T The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Ca...](https://isitonrecall.com/recall/fda-device-z-0627-2022-arrow-trerotola-ptd-set-percutaneous-thrombolytic-device-pt-45509-containing-components-pt-45509-s6/) The firm received reports indicating PTD tip separation during use. Class I Reported terminated Distribution: Worldwide distribution: US Nationwide and the countries of AU, BE, CA, CL, CZ, DE, ES, FR, GB, IL, IT, KR, KW, NL, PA, PH, PT, SA, TR. [Official source for Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), PT-45509 containing components: PT-45...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0627-2022%22) Jan 11, 2022 FDA device enforcement ### [5 Fr. X 65 cm Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device, REF PT-65509-HFC containing components: PT-03000, PT-65509-S (PT-65509-S2 alternative), PT-01000-D (PT-0...](https://isitonrecall.com/recall/fda-device-z-0628-2022-5-fr-x-65-cm-arrow-trerotola-ptd-kit-percutaneous-thrombolytic-device-ref-pt-65509-hfc-containing-co/) The firm received reports indicating PTD tip separation during use. Class I Reported terminated Distribution: Worldwide distribution: US Nationwide and the countries of AU, BE, CA, CL, CZ, DE, ES, FR, GB, IL, IT, KR, KW, NL, PA, PH, PT, SA, TR. [Official source for 5 Fr. X 65 cm Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device, REF PT-65509-HFC contain...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0628-2022%22) Jan 11, 2022 FDA device enforcement ### [Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), REF PT-65509 (finished good kit) The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction ...](https://isitonrecall.com/recall/fda-device-z-0629-2022-arrow-trerotola-ptd-set-percutaneous-thrombolytic-device-ref-pt-65509-finished-good-kit-the-arrow-tr/) The firm received reports indicating PTD tip separation during use. Class I Reported terminated Distribution: Worldwide distribution: US Nationwide and the countries of AU, BE, CA, CL, CZ, DE, ES, FR, GB, IL, IT, KR, KW, NL, PA, PH, PT, SA, TR. [Official source for Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), REF PT-65509 (finished good kit) The ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0629-2022%22) ## Reasons in these listed records - Reports received of torn corrugated breathing tubes. - The firm received reports indicating PTD tip separation during use. These examples come from this result page and are not a ranking of every recall reason. ## Checking TELEFLEX MEDICAL INC ### Is there a recall on teleflex medical inc right now? This archive contains 9 records, including 2 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 TELEFLEX MEDICAL INC](https://isitonrecall.com/check/?q=TELEFLEX%20MEDICAL%20INC) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)