Recall: Baxter Sodium Chloride Injection
On 2014-09-15, the FDA announced that Baxter is conducting a recall on Sodium Chloride Injection due to possible contamination with foreign matter. The recalled products were sold under the brand name(s) Baxter from 2014 to 2014 throughout the regions shown in the map below.
In recent months, there have been 10 drugs recalls due to potential contamination, including heparin sodium, peritoneal dialysis solution and more. Additionally, there have been 7 drug and medical device recalls due to other health hazards as well as 143 food recalls.
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Detailed Recall Information
Regions Where Sold: Nationwide
Product Description: Sodium Chloride Injection
Brand Name(s): Baxter
Dates Sold: 2014
Reason for Recall: Particulate matter
Official Recall Date: 2014-06-24
Additional information provided by the FDA.gov:
Baxter International Inc. announced today it is voluntarily recalling one lot of 0.9% Sodium Chloride Injection, USP 1000 mL, a portion of which was released to customers. The recall is being initiated as a result of particulate matter found near the administration port. Read More.
More information may be available at FDA.gov
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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.