Cordis US Corp recalls Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN
Recalled Product
Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
Hazard / Issue
Non-sterile product labeled as sterile was distributed.
Issued by
FDA
Affected States: OK
Lot/Code Info: UDI/DI 10705032025935, Lot Number 18223410
View official government recall
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