FDA-Device2023-11-15Class I

Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter

Cordis US Corp
Hazard

Non-sterile product labeled as sterile was distributed.

Sold states
US Distribution to: OK
Affected count
30 devices
Manufactured in
14201 Nw 60th Ave, Miami Lakes, FL, United States
Products
Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0286-2024

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief