Brand

Cordis Us Corp Recalls

9 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Cordis Us Corp.

9Total Recalls
6Critical
1,035Units Affected
Mar 4, 2025Most Recent
All Recalls

Every Cordis Us Corp Recall

Sorted by most recent. Click any recall for full details.

9 recalls
High RiskFDA
Cordis Us Corp
Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only
Medical Implants·20 affected·Mar 4, 2025
High RiskFDA
Cordis Us Corp
Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introd...
Surgical Devices·12 affected·Feb 7, 2025
High RiskFDA
Cordis Us Corp
MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites.
Medical Devices·50 affected·Nov 28, 2023
CriticalFDA
Cordis Us Corp
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC
Medical Devices·40 affected·Mar 24, 2023
CriticalFDA
Cordis Us Corp
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM
Medical Devices·56 affected·Mar 24, 2023
CriticalFDA
Cordis Us Corp
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC
Medical Devices·146 affected·Mar 24, 2023
CriticalFDA
Cordis Us Corp
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM
Medical Devices·27 affected·Mar 24, 2023
CriticalFDA
Cordis Us Corp
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM
Medical Devices·0 affected·Mar 24, 2023
CriticalFDA
Cordis Us Corp
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC
Medical Devices·684 affected·Mar 24, 2023