--- title: "Galt Medical Corporation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Galt Medical Corporation recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/galt-medical-corporation/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Galt Medical Corporation recall records **10** reported ongoing 10 records in this archive. Latest source date Jun 26, 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 26, 2026 FDA device enforcement ### [Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator , Stiffen Dilator, Nitinol Mandrel Wire w/ Radiopaque Tip (Au}, ...](https://isitonrecall.com/recall/fda-device-z-2917-2026-boston-scientific-enhance-transcarotid-peripheral-access-kit-ref-sr-4f21g7d-mp-kit-075-03-sheath-wit/) Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits. Class II Reported ongoing Distribution: US Nationwide distribution in the state of MN. [Official source for Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Shea...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2917-2026%22) Mar 27, 2025 FDA device enforcement ### [GALT Centeze Catheter REF: DRC-002-05 DRC-002-06 The Centeze is intended for use in percutaneous fluid aspirations and small volume drainage procedures. For both adult and adole...](https://isitonrecall.com/recall/fda-device-z-1731-2025-galt-centeze-catheter-ref-drc-002-05-drc-002-06-the-centeze-is-intended-for-use-in-percutaneous-flui/) Due to a potential open seal in the sterile barrier packaging . Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of AL, FL, GA, IL, MA, OH, PA, and UT. The countries of Canada, Ireland, Israel, Korea, Qatar, and United Kingdom. [Official source for GALT Centeze Catheter REF: DRC-002-05 DRC-002-06 The Centeze is intended for use in percutaneous ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1731-2025%22) Mar 27, 2025 FDA device enforcement ### [B Braun Interventional Coaxial Dilator REF: KIT-018-47, KIT-019-67, KIT-018-41, KIT-019-37 These Micro-Introducer Kits are intended to introduce up to a .038 inch guidewire or c...](https://isitonrecall.com/recall/fda-device-z-1732-2025-b-braun-interventional-coaxial-dilator-ref-kit-018-47-kit-019-67-kit-018-41-kit-019-37-these-micro-i/) Due to a potential open seal in the sterile barrier packaging . Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of AL, FL, GA, IL, MA, OH, PA, and UT. The countries of Canada, Ireland, Israel, Korea, Qatar, and United Kingdom. [Official source for B Braun Interventional Coaxial Dilator REF: KIT-018-47, KIT-019-67, KIT-018-41, KIT-019-37 These ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1732-2025%22) Mar 27, 2025 FDA device enforcement ### [B Braun Interventional ELITE HV Hemostasis Valve Introducer System REF 612802 Model Number: BCL-100-04 The Elite HV¿ Introducer System is indicated for use in percutaneous proce...](https://isitonrecall.com/recall/fda-device-z-1733-2025-b-braun-interventional-elite-hv-hemostasis-valve-introducer-system-ref-612802-model-number-bcl-100-0/) Due to a potential open seal in the sterile barrier packaging . Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of AL, FL, GA, IL, MA, OH, PA, and UT. The countries of Canada, Ireland, Israel, Korea, Qatar, and United Kingdom. [Official source for B Braun Interventional ELITE HV Hemostasis Valve Introducer System REF 612802 Model Number: BCL-1...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1733-2025%22) Mar 27, 2025 FDA device enforcement ### [GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to introduce and position catheters and other interventional devices within the Coronar...](https://isitonrecall.com/recall/fda-device-z-1734-2025-galt-guidewire-ref-sgw-051-07-guidewires-are-intended-for-use-in-percutaneous-procedures-to-introduc/) Due to a potential open seal in the sterile barrier packaging. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of AL, FL, GA, IL, MA, OH, PA, and UT. The countries of Canada, Ireland, Israel, Korea, Qatar, and United Kingdom. [Official source for GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to intr...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1734-2025%22) Mar 27, 2025 FDA device enforcement ### [Introducer Kit- Coaxial Dilator REF: KIT-002-28, 00841268104730 KIT-002-34, 00841268104792 KIT-002-35, 00841268104808 KIT-011-40, 00841268105553 KIT-011-62, 00841268105614 KIT-0...](https://isitonrecall.com/recall/fda-device-z-1735-2025-introducer-kit-coaxial-dilator-ref-kit-002-28-00841268104730-kit-002-34-00841268104792-kit-002-35-00/) Due to a potential open seal in the sterile barrier packaging. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of AL, FL, GA, IL, MA, OH, PA, and UT. The countries of Canada, Ireland, Israel, Korea, Qatar, and United Kingdom. [Official source for Introducer Kit- Coaxial Dilator REF: KIT-002-28, 00841268104730 KIT-002-34, 00841268104792 KIT-00...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1735-2025%22) Mar 27, 2025 FDA device enforcement ### [Introducer Needle REF NDL-107-04 These needles are used for the percutaneous introduction of guidewires](https://isitonrecall.com/recall/fda-device-z-1736-2025-introducer-needle-ref-ndl-107-04-these-needles-are-used-for-the-percutaneous-introduction-of-guidewi/) Due to a potential open seal in the sterile barrier packaging. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of AL, FL, GA, IL, MA, OH, PA, and UT. The countries of Canada, Ireland, Israel, Korea, Qatar, and United Kingdom. [Official source for Introducer Needle REF NDL-107-04 These needles are used for the percutaneous introduction of guid...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1736-2025%22) Mar 27, 2025 FDA device enforcement ### [Introducer Kit- Tearaway MicroSlide REF KIT-051-01, 00841268106130 INT-101-15, 00841268107380 These introducers are used for the procedures to introduce catheters and other intr...](https://isitonrecall.com/recall/fda-device-z-1737-2025-introducer-kit-tearaway-microslide-ref-kit-051-01-00841268106130-int-101-15-00841268107380-these-int/) Due to a potential open seal in the sterile barrier packaging. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of AL, FL, GA, IL, MA, OH, PA, and UT. The countries of Canada, Ireland, Israel, Korea, Qatar, and United Kingdom. [Official source for Introducer Kit- Tearaway MicroSlide REF KIT-051-01, 00841268106130 INT-101-15, 00841268107380 The...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1737-2025%22) May 8, 2023 FDA device enforcement ### [Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16](https://isitonrecall.com/recall/fda-device-z-1968-2023-tearaway-introducer-kit-ref-kit-010-12-kit-010-17-kit-900-16/) Sheath introducer assemblies could potentially, due to improper storage conditions, have a luer connection portion of the dilator hub that cracks or dislodges during use, which renders the dilator component unusable, and can require the use of a replacement... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of PA, UT, FL, PA, OH, GA, MA, NV, CA, NY, NJ and the countries of UK, AU, TR, FR, CH, NO. [Official source for Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1968-2023%22) May 8, 2023 FDA device enforcement ### [Tearaway Introducer Set, REF: INT-028-27, INT-105-25, INT-106-09, INT-106-12, INT-106-17, DSS-007-04, DSS-007-05, DSS-010-065, DSS-012-07 (bulk)](https://isitonrecall.com/recall/fda-device-z-1969-2023-tearaway-introducer-set-ref-int-028-27-int-105-25-int-106-09-int-106-12-int-106-17-dss-007-04-dss-00/) Sheath introducer assemblies could potentially, due to improper storage conditions, have a luer connection portion of the dilator hub that cracks or dislodges during use, which renders the dilator component unusable, and can require the use of a replacement... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of PA, UT, FL, PA, OH, GA, MA, NV, CA, NY, NJ and the countries of UK, AU, TR, FR, CH, NO. [Official source for Tearaway Introducer Set, REF: INT-028-27, INT-105-25, INT-106-09, INT-106-12, INT-106-17, DSS-007...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1969-2023%22) ## Reasons in these listed records - Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits. - Due to a potential open seal in the sterile barrier packaging . - Due to a potential open seal in the sterile barrier packaging. - Sheath introducer assemblies could potentially, due to improper storage conditions, have a luer connection portion of the dilator hub that cracks or dislodges during use, which renders the dilator component unusable, and can require the use of a replacement device. These examples come from this result page and are not a ranking of every recall reason. ## Checking Galt Medical Corporation ### Is there a recall on galt medical corporation right now? This archive contains 10 records, including 10 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 Galt Medical Corporation](https://isitonrecall.com/check/?q=Galt%20Medical%20Corporation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)