Cordis Us recalls
Cordis Us appears in 22 official U.S. recall notices indexed by RecallRadar, most recently on 2025-04-09.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only
FDA Device · Class II · 2025-04-09 · Cordis Us - Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only
FDA Device · Class II · 2025-04-09 · Cordis Us - Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduct…
FDA Device · Class II · 2025-03-19 · Cordis Us - MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites
FDA Device · Class II · 2024-01-17 · Cordis Us - MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites
FDA Device · Class II · 2024-01-17 · Cordis Us - Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
FDA Device · Class I · 2023-11-15 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC
FDA Device · Class I · 2023-05-17 · Cordis Us - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE
FDA Device · Class I · 2023-05-17 · Cordis Us - Cordis Angiographic Catheter Extensions
FDA Device · Class II · 2022-12-21 · Cordis Us - PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX, PG3990BPS, PG3990BPX
FDA Device · Class II · 2022-07-20 · Cordis Us