Cordis US Recalls
22 recalls on record · July 20, 2022 to April 9, 2025 · Medical Devices
Recalls by year
22
23
24
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 9, 2025Medical DevicesFDA
Cordis US Corp recalls Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only
Hazard: product mix-up; Vascular stent labeled as one size but contains a different size.
April 9, 2025Medical DevicesFDA
Cordis US Corp recalls Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only
Hazard: product mix-up; Vascular stent labeled as one size but contains a different size.
March 19, 2025Medical DevicesFDA
Cordis US Corp recalls Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for int
Hazard: Catheter manufactured at the incorrect length.
January 17, 2024Medical DevicesFDA
Cordis US Corp recalls MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites
Hazard: 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, MynxGrip 6/7F) was labeled as F2322902 (Item MX5021, MynxGrip 5F). The primary label on individual devices is correct.
January 17, 2024Medical DevicesFDA
Cordis US Corp recalls MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites.
Hazard: 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, MynxGrip 6/7F) was labeled as F2322902 (Item MX5021, MynxGrip 5F). The primary label on individual devices is correct.
November 15, 2023Medical DevicesFDA
Cordis US Corp recalls Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
Hazard: Non-sterile product labeled as sterile was distributed.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC
Hazard: 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 device is prepared.
May 17, 2023Medical DevicesFDA
Cordis US Corp recalls ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC
Hazard: 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 device is prepared.
December 21, 2022Medical DevicesFDA
Cordis US Corp recalls Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for inject
Hazard: There is a potential for separation at the male connector.
July 20, 2022Medical DevicesFDA
Cordis US Corp recalls PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX, PG399
Hazard: Potential for stent dislodgement and associated failures related to two specific sizes of the device.