Cordis US Corp: Medical Device Recalls in 2023
Updated on March 25, 2026.
According to to data from the FDA, there were 15 medical device recalls made by Cordis US Corp in 2023. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC
- ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC