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Cordis Corporation recalls PRECISE PRO RX CAROTID STENT implant system, Product Codes: PC0520RXC, PC0530RXC, PC0540RXC, PC0620RXC, PC0630RXC, PC06
Recalled March 24, 2021 · FDA recall Z-1257-2021 · Cordis
Hazard
Distal tip may become separated from the lumen wire in specific lots. · FDA Class I
Units
18218 units
Sold at
US (except MT and NM) and Taiwan
Description
Distal tip may become separated from the lumen wire in specific lots.
Product
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
Manufacturer(s)
Cordis Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →