Every recall we track for Cordis US Corp — 22 in all — plus the complaints and injury reports the public filed about them.
Cordis recalls specific Smart Control Vascular Stent System models due to size mix-up risk. This could lead to incorrect implantation during procedures.
Cordis recalls Smart Control Vascular Stent System ILIAC 10mm X 40mm 6F due to size mix-up. This could lead to incorrect stent placement during surgery.
Cordis recalls Vista Brite Tip catheters with incorrect length. This may cause improper use during medical procedures. Affected units have specific UDI and lot numbers.
Cordis recalls MYNXGRIP 6F/7F vascular closure devices due to incorrect carton labels for some lots. Affected units may have wrong lot numbers, but individual device labels are correct.
Cordis recalls MYNXGRIP 5F vascular closure devices due to incorrect lot numbers on carton boxes. This mix-up may cause confusion but does not pose a safety risk to users.
Cordis recalls cardiac catheter sets with non-sterile product labeled as sterile. Affected units include specific model and lot numbers. No remedy details provided in recall notice.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with potential separation during procedures, risking stroke or complications. Affected units have specific lot numbers and UDI/DI codes.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with specific lot numbers due to potential separation during medical procedures, which could lead to stroke or other complications.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with potential separation during procedures, risking stroke or complications. Affected units have specific lot numbers and reference codes.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with specific lot numbers due to potential separation during medical procedures, which could lead to stroke or other complications.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with specific lot numbers due to potential separation during medical procedures, which could lead to complications like stroke.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with specific lot numbers due to potential separation during medical procedures, which could lead to stroke or other complications.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with specific lot numbers due to potential separation during medical procedures, which could lead to stroke or other complications.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with potential separation during procedures, risking stroke or complications. Affected units include specific model and lot numbers.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with specific lot numbers due to potential separation during medical procedures, which could lead to stroke or other complications.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with potential separation during procedures, risking stroke or complications. Affected units include specific lot numbers and reference codes.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with specific lot numbers due to potential separation during medical procedures, which could lead to complications like stroke.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with specific lot numbers due to potential separation during medical procedures, which could lead to stroke or other complications.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with potential separation during procedures, risking stroke or complications. Affected units include specific lot numbers and reference codes.
Cordis recalls ANGIOGUARD RX/XP Emboli Capture Guidewire Systems with potential separation during medical procedures, risking stroke or complications. Affected units include specific lot numbers and reference codes.
Cordis recalls angiographic catheter extensions with a potential male connector separation hazard. Affected units have specific catalog numbers and lot numbers. Consumers should contact Cordis for details.
Cordis recalls specific PALMAZ Genesis Transhepatic Biliary Stent models due to potential dislodgement. Affected units have catalog numbers PG2990BPS, PG2990BPX, PG3990BPS, PG3990BPX with listed lot numbers and expiration dates.
