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Hospira Lactated Ringer’s and 5% Dextrose Injection Recalled: AttorneyOne Monitor and Keep Consumers Informed
Date:7/14/2014

San Diego, CA (PRWEB) July 14, 2014

AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Hospira Lactated Ringer’s and 5% Dextrose Injection.

The FDA informed on July 11, that one lot of Lactated Ringers and 5% Dextrose Injection, USP, 1000 mL, Flexible Container, by Hospira Inc., is recalled due to mold contamination. The specific product is used for parenteral replacement of extracellular losses of fluid and electrolytes, with or without minimal carbohydrate calories.

The reason for the recall is based on a confirmed customer report where particulate was identified as a filamentous-like structured particulate indicative of mold. Administration of the specific product can lead to infections, even life-threatening, and may cause prolonged hospitalization or organ fail
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