NEW YORK --
One lot of Zicam Extreme Congestion Relief nasal gel has been recalled by its manufacturer after routine testing revealed Burkholderia cepacia bacteria in a sample, the U.S. Food and Drug Administration reported.
The company, Matrixx Initiatives, said the affected lot had been distributed nationwide. The lot consists of 0.5-ounce spray bottles containing a nondrip liquid, in cartons labeled with NDC number 62750-005-10, lot number 2J23, with an expiration date of September 2015.
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