Cordis US recalls

Cordis US has 22 recalls on record with the FDA and USDA, the earliest in 2022 and the latest reported on 9 Apr 2025. 22 are still ongoing.

Total recalls22since 2022

Last 12 months0reported

Class I1568% of total

Ongoing22latest 9 Apr 2025

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 1 2 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 15 68%Class II 7 32%Class III 0 0%

Why cordis us is recalled

Product types

Heart & Vascular Devices22100%

By year

2025314%
202429%
20231568%
202229%

Ongoing cordis us recalls

22 active

Reported	Class	Recall	Company	Reason	Where
9 Apr 2025Device	CLASS II	Cordis, REF: C09060ML, Smart Control Vascular Stent System recalled	Cordis US	Packaging Defects	5 states
9 Apr 2025Device	CLASS II	Cordis, REF C10040ML, Smart Control Vascular Stent System recalled	Cordis US	Packaging Defects	5 states
19 Mar 2025Device	CLASS II	Vista Brite Tip, Judkins Right recalled by Cordis US	Cordis US	Other	WA
17 Jan 2024Device	CLASS II	Mynxgrip 6f/7f recalled by Cordis US	Cordis US	Packaging Defects	7 states
17 Jan 2024Device	CLASS II	Mynxgrip 5F recalled by Cordis US	Cordis US	Packaging Defects	7 states
15 Nov 2023Device	CLASS I	Cordis Angiographic Catheterization Sets, Infiniti Thrulemen, 5F recalled	Cordis US	Sterility	OK

All cordis us recalls, newest first

22 total

Reported	Class	Recall	Company	Reason	Where
9 Apr 2025Device	CLASS II	Cordis, REF: C09060ML, Smart Control Vascular Stent System recalled	Cordis US	Packaging Defects	5 states
9 Apr 2025Device	CLASS II	Cordis, REF C10040ML, Smart Control Vascular Stent System recalled	Cordis US	Packaging Defects	5 states
19 Mar 2025Device	CLASS II	Vista Brite Tip, Judkins Right recalled by Cordis US	Cordis US	Other	WA
17 Jan 2024Device	CLASS II	Mynxgrip 6f/7f recalled by Cordis US	Cordis US	Packaging Defects	7 states
17 Jan 2024Device	CLASS II	Mynxgrip 5F recalled by Cordis US	Cordis US	Packaging Defects	7 states
15 Nov 2023Device	CLASS I	Cordis Angiographic Catheterization Sets, Infiniti Thrulemen, 5F recalled	Cordis US	Sterility	OK
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
17 May 2023Device	CLASS I	Angioguard RX / XP Emboli Capture Guidewire System recalled by Cordis US	Cordis US	Other	FL
21 Dec 2022Device	CLASS II	Cordis Angiographic Catheter Extensions recalled by Cordis US	Cordis US	Other	Nationwide
20 Jul 2022Device	CLASS II	Palmaz Genesis Transhepatic Biliary Stent on Opta Pro .035" recalled	Cordis US	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.