FDAFebruary 11, 2021device
PRECISE PRO RX CAROTID STENT implant system, Product Codes: PC0520RXC, PC0530RXC, PC0540RXC, PC0620RXC, PC0630RXC, PC0640RXC, PC0720RXC, PC0730RXC, PC0740RXC, PC0820RXC, PC0830RXC, PC0840RXC, PC0920RXC, PC0930RXC, PC0940RXC, PC1030RXC, PC1040RXC
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Distal tip may become separated from the lumen wire in specific lots.
What to do
FDA enforcement status: Completed
Brands named
cordis
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDACordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only2025-03-04
- FDACordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only2025-03-04
- FDAVista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.2025-02-07
- FDAMYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites.2023-11-28
- FDAMYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites2023-11-28
- FDACordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter2023-09-26
- FDAANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM2023-03-24
- FDAANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC2023-03-24
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