--- title: "Cordis US Corp Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Cordis US Corp recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/cordis-us-corp/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Cordis US Corp recall records **22** reported ongoing 22 records in this archive. Latest source date Mar 4, 2025. 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 Mar 4, 2025 FDA device enforcement ### [Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only](https://isitonrecall.com/recall/fda-device-z-1510-2025-cordis-ref-c10040ml-smart-control-vascular-stent-system-iliac-10mm-x-40mm-6f-sterileeo-rx-only/) product mix-up; Vascular stent labeled as one size but contains a different size. Class II Reported ongoing Distribution: US Distribution to states of: AR, AZ, FL, NJ, TN; and OUS Foreign country of: Japan [Official source for Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1510-2025%22) Mar 4, 2025 FDA device enforcement ### [Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only](https://isitonrecall.com/recall/fda-device-z-1511-2025-cordis-ref-c09060ml-smart-control-vascular-stent-system-iliac-9mm-x-60mm-6f-sterileeo-rx-only/) product mix-up; Vascular stent labeled as one size but contains a different size. Class II Reported ongoing Distribution: US Distribution to states of: AR, AZ, FL, NJ, TN; and OUS Foreign country of: Japan [Official source for Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1511-2025%22) Feb 7, 2025 FDA device enforcement ### [Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devic...](https://isitonrecall.com/recall/fda-device-z-1330-2025-vista-brite-tip-judkins-right-4-ref-sm7504-jr3-vbt-special-110-cm-6f-guiding-catheter-is-intended-fo/) Catheter manufactured at the incorrect length. Class II Reported ongoing Distribution: US: WA OUS: Japan [Official source for Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is in...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1330-2025%22) Nov 28, 2023 FDA device enforcement ### [MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites.](https://isitonrecall.com/recall/fda-device-z-0674-2024-mynxgrip-5f-ref-mx5021-vascular-closure-device-vcd-used-to-seal-femoral-arterial-and-femoral-venous/) Cordis became aware that the label for the carton box containing 10 units is incorrect for some boxes of two lots of MynxGrip. The carton box from lot F2322902 (Item MX5021, MynxGrip 5F) as labeled as lot F2322903 (MX6721, MynxGrip 6/7F) and product from lo... Class II Reported ongoing Distribution: US: NC, WV, TN, MS, MI, OH, CA [Official source for MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0674-2024%22) Nov 28, 2023 FDA device enforcement ### [MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites](https://isitonrecall.com/recall/fda-device-z-0675-2024-mynxgrip-6f-7f-ref-mx6721-vascular-closure-device-vcd-used-to-seal-femoral-arterial-and-femoral-veno/) Cordis became aware that the label for the carton box containing 10 units is incorrect for some boxes of two lots of MynxGrip. The carton box from lot F2322902 (Item MX5021, MynxGrip 5F) as labeled as lot F2322903 (MX6721, MynxGrip 6/7F) and product from lo... Class II Reported ongoing Distribution: US: NC, WV, TN, MS, MI, OH, CA [Official source for MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femo...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0675-2024%22) Sep 26, 2023 FDA device enforcement ### [Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter](https://isitonrecall.com/recall/fda-device-z-0286-2024-cordis-angiographic-catheterization-sets-infiniti-thrulemen-5f-ref-co0208-cardiac-catheter/) Non-sterile product labeled as sterile was distributed. Class I Reported ongoing Distribution: US Distribution to: OK [Official source for Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0286-2024%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC](https://isitonrecall.com/recall/fda-device-z-1483-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-401814rmc/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1483-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC](https://isitonrecall.com/recall/fda-device-z-1484-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-501814rmc/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1484-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC](https://isitonrecall.com/recall/fda-device-z-1485-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-601814rmc/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1485-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC](https://isitonrecall.com/recall/fda-device-z-1486-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-701814rmc/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1486-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC](https://isitonrecall.com/recall/fda-device-z-1487-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-801814rmc/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1487-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC](https://isitonrecall.com/recall/fda-device-z-1488-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-603014mc/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1488-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC](https://isitonrecall.com/recall/fda-device-z-1489-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-501814rec/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1489-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM](https://isitonrecall.com/recall/fda-device-z-1490-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-401814rm/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1490-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE](https://isitonrecall.com/recall/fda-device-z-1491-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-501814re/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1491-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE](https://isitonrecall.com/recall/fda-device-z-1492-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-601814re/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1492-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE](https://isitonrecall.com/recall/fda-device-z-1493-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-701814re/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1493-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM](https://isitonrecall.com/recall/fda-device-z-1494-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-601814rm/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1494-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM](https://isitonrecall.com/recall/fda-device-z-1495-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-501814rm/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1495-2023%22) Mar 24, 2023 FDA device enforcement ### [ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE](https://isitonrecall.com/recall/fda-device-z-1496-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-801814re/) There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de... Class I Reported ongoing Distribution: Worldwide distribution. [Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1496-2023%22) ## Reasons in these listed records - product mix-up; Vascular stent labeled as one size but contains a different size. - Catheter manufactured at the incorrect length. - Cordis became aware that the label for the carton box containing 10 units is incorrect for some boxes of two lots of MynxGrip. The carton box from lot F2322902 (Item MX5021, MynxGrip 5F) as labeled as lot F2322903 (MX6721, MynxGrip 6/7F) and product from lot F2322903 (MX6721, ... - Non-sterile product labeled as sterile was distributed. These examples come from this result page and are not a ranking of every recall reason. ## Checking Cordis US Corp ### Is there a recall on cordis us corp right now? This archive contains 22 records, including 22 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 Cordis US Corp](https://isitonrecall.com/check/?q=Cordis%20US%20Corp) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)