FDA-Device2023-06-14Class II

Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G

C.R. Bard Inc
Hazard

Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.

Sold states
Worldwide
Affected count
5760 devices
Manufactured in
8195 Industrial Blvd Ne, Covington, GA, United States
Products
Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1700-2023

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