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Home > Recalled Products > Drugs > Contamination > Baxter 0.9% Sodium Chloride Injection USP

Recall: Baxter 0.9% Sodium Chloride Injection USP


On 2014-12-15, the FDA announced that Baxter International is conducting a recall on 0.9% Sodium Chloride Injection USP due to possible contamination with foreign matter. The recalled products were sold under the brand name(s) Baxter during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 5 drugs recalls due to potential contamination, including dietary supplement, containers and more. Additionally, there have been 8 drug and medical device recalls due to other health hazards as well as 86 food recalls.

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Baxter recalls Sodium Chloride Injection

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Company Contact Information:

Name: Baxter International
Phone: 800-422-9837

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Detailed Recall Information

Regions Where Sold: Nationwide

Product Description: 0.9% Sodium Chloride Injection USP

Brand Name(s): Baxter

Reason for Recall: Contains Particulate Matter

Official Recall Date: 2014-12-11

Note: Although this recall announcement is dated 12/11/2014, it was not published by the FDA until 12/15/2014.


Additional information provided by the

Baxter International Inc. announced today it voluntarily initiated a recall in the United States of two lots of 0.9% Sodium Chloride Injection USP in 100 mL MINI-BAG PLUS Container to the hospital/user level. The recall is being initiated as a result of two complaints (one per lot) of particulate matter that was identified as a fragment of the frangible from the vial adapter. The issue was identified upon standard visual inspection prior to patient administration. Read More.

More information may be available at

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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.

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