Vials of the hepatitis B vaccine RECOMBIVAX HB are being recalled by the manufacturer because a limited number of the vials in the lot may crack, the Food and Drug Administration (FDA) announced. If a crack occurs, the integrity of the vial and the sterility of any product remaining in the vial could not be assured. Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., issued the recall for Lot Number J001183 of RECOMBIVAX HB (Recombinant) Adult Formulation. The product was distributed only in the United States between March 12, 2013, and May 2, 2013. The company says ... Read More
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