FDA-Drug2013-07-03Class II

5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7926-48

Hospira Inc.
Hazard

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Sold states
Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia
Affected count
74,256 units
Manufactured in
275 N Field Dr, Lake Forest, IL, United States
Products
5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7926-48

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-615-2013

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