0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, ...
FDA Recall #D-0334-2015 — Class II — December 22, 2014
Product Description
0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11
Reason for Recall
Lack of Assurance of Sterility: The product has the potential for solution to leak at the administrative port.
Recalling Firm
Hospira Inc. — Lake Forest, IL
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Drugs
Product Quantity
30840 bags
Distribution
Nationwide
Code Information
Lot #: 42-306-C6
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated