--- title: "Atrium Medical Corporation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Atrium 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/atrium-medical-corporation/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Atrium Medical Corporation recall records **87** reported ongoing 87 records in this archive. Latest source date Aug 7, 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 Aug 7, 2026 FDA device enforcement ### [Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Number): 1. 16FR(8016), 2. 24FR(8024), 3. 28FR(8028), 4. 32FR(8032), 5. 36FR(8036);](https://isitonrecall.com/recall/fda-device-z-3111-2026-getinge-pvc-thoracic-catheter-soft-pvc-straight-10-per-case-size-model-number-1-16fr-8016-2-24fr-802/) An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Number): 1. 16FR(8016),...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3111-2026%22) Aug 7, 2026 FDA device enforcement ### [Getinge PVC Thoracic Catheter, Soft PVC Right Angle, 10 per Case; Size(Model Number): 1. 24FR(8124), 2. 28FR(8128), 3. 32FR(8132), 4. 36FR(8136);](https://isitonrecall.com/recall/fda-device-z-3112-2026-getinge-pvc-thoracic-catheter-soft-pvc-right-angle-10-per-case-size-model-number-1-24fr-8124-2-28fr/) An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Getinge PVC Thoracic Catheter, Soft PVC Right Angle, 10 per Case; Size(Model Number): 1. 24FR(812...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3112-2026%22) Aug 7, 2026 FDA device enforcement ### [Getinge PVC Thoracic Catheter, Firm PVC Straight, 10 per Case; Size(Model Number): 1. 28FR(15028), 2. 36FR(15036);](https://isitonrecall.com/recall/fda-device-z-3113-2026-getinge-pvc-thoracic-catheter-firm-pvc-straight-10-per-case-size-model-number-1-28fr-15028-2-36fr-15/) An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Getinge PVC Thoracic Catheter, Firm PVC Straight, 10 per Case; Size(Model Number): 1. 28FR(15028)...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3113-2026%22) Sep 9, 2024 FDA device enforcement ### [iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616](https://isitonrecall.com/recall/fda-device-z-0024-2025-icast-covered-stent-6mmx16mmx120cm-model-number-42616/) There is an error in the Unique Device Identifier (UDI) printed on the product's distribution label. Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, MA, MI, OH, WA. [Official source for iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0024-2025%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 5X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1951-2024-advanta-vxt-5x40-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 5X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1951-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 6X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1952-2024-advanta-vxt-6x40-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 6X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1952-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 8X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1953-2024-advanta-vxt-8x40-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 8X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1953-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 5X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1954-2024-advanta-vxt-5x50-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 5X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1954-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 6X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1955-2024-advanta-vxt-6x50-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 6X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1955-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 7X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1956-2024-advanta-vxt-7x50-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 7X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1956-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 8X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1957-2024-advanta-vxt-8x50-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 8X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1957-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 5X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1958-2024-advanta-vxt-5x70-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 5X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1958-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 6X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1959-2024-advanta-vxt-6x70-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 6X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1959-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 7X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1960-2024-advanta-vxt-7x70-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 7X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1960-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 8X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1961-2024-advanta-vxt-8x70-1gds-nh-str-sw-single-ended-slider-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 8X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1961-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 5X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1962-2024-advanta-vxt-5x40-1gds-fh-str-sw-single-ended-slider-gds-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 5X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1962-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 6X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1963-2024-advanta-vxt-6x40-1gds-fh-str-sw-single-ended-slider-gds-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 6X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1963-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 5X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1964-2024-advanta-vxt-5x50-1gds-fh-str-sw-single-ended-slider-gds-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 5X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1964-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 6X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1965-2024-advanta-vxt-6x50-1gds-fh-str-sw-single-ended-slider-gds-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 6X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1965-2024%22) May 3, 2024 FDA device enforcement ### [ADVANTA VXT, 7X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft](https://isitonrecall.com/recall/fda-device-z-1966-2024-advanta-vxt-7x50-1gds-fh-str-sw-single-ended-slider-gds-vascular-graft/) Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB... [Official source for ADVANTA VXT, 7X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1966-2024%22) ## Reasons in these listed records - An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - There is an error in the Unique Device Identifier (UDI) printed on the product's distribution label. - Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. These examples come from this result page and are not a ranking of every recall reason. ## Checking Atrium Medical Corporation ### Is there a recall on atrium medical corporation right now? This archive contains 87 records, including 87 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 Atrium Medical Corporation](https://isitonrecall.com/check/?q=Atrium%20Medical%20Corporation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)