FDAClass IISeptember 26, 2018

0.9% Sodium Chloride Injection USP recall: CGMP Deviations

0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Healthcare Corporation Deerfield, IL 60015 -- NDC 0338-0049-31

Why was 0.9% Sodium Chloride Injection USP recalled?

cGMP Deviation

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot: P380063 Exp. 12/2019

Product
0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Healthcare Corporation Deerfield, IL 60015 -- NDC 0338-0049-31
Recalling firm
Baxter Healthcare Corporation
Quantity
5184 bags
Distribution
Nationwide.
Recall date
September 26, 2018
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls