Hospira Recalls IV Solution over Mold Concerns
Hospira Inc. initiated a nationwide recall for one lot of an intravenous solution after receiving a customer report of a spore-like matter resembling a mold found in the solution. The recalled product is called Lactated Ringers and 5% Dextrose Injection, according to the U.S. Food and Drug Administration (FDA). It is used as a source of water, electrolytes, and calories or as an alkalizing agent in patients. The details of the packaging of the recalled lot of 5% Dextrose Injection include: • 1000 ml flexible container • lot number: