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Cordis US Corp recalls Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
Recalled November 15, 2023 · FDA recall Z-0286-2024 · Cordis US
Hazard
Non-sterile product labeled as sterile was distributed. · FDA Class I
Units
30 devices
Sold at
US Distribution to: OK
Description
Non-sterile product labeled as sterile was distributed.
Product
Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
Manufacturer(s)
Cordis US Corp
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →