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: Illinois Injury Lawyer BlogFDA and Bayer issue product recall for Alka-Seltzer capsules with wrong label
The Food and Drug Administration (FDA) and Bayer have issued a voluntary recall for gel capsules of Alka Seltzer that have the wrong labeling. The product recall affects the combination package of Alka-Seltzer Plus Day and Night Cold Formula Liquid Gels. The product recall was initiated when the company found out that the labeling was printed reversed last week.
Full post as published by Illinois Injury Lawyer Blog on December 18, 2009 (boomark / email).
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