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

0Oct '24 0 0 0Jan '25 0 1 2Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 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	Sterility	5 states
9 Apr 2025Device	CLASS II	Cordis, REF C10040ML, Smart Control Vascular Stent System recalled	Cordis US	Sterility	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	Sterility	5 states
9 Apr 2025Device	CLASS II	Cordis, REF C10040ML, Smart Control Vascular Stent System recalled	Cordis US	Sterility	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

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.