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February 4, 2012

American Regent Initiates Nationwide Voluntary Recall of Sterile Water for Injection, USP 50 mL Single Dose Vial Due to Particulate Matter

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Shirley, NY – American Regent is conducting a nationwide voluntary recall to the consumer and user level of the following product: Sterile Water for Injection, USP, 50 mL Single Dose Vial, NDC # 0517-3050-25, Lot 0092, Exp. Date February, 2014 PLEASE NOTE: This recall, initiated on May 19, 2011 to the User or Consumer Level, [...]

Lilly Announces Important Action Regarding Recall of Alcohol Prep Pads Made by Triad Group Included in Forteo Starter Kits

INDIANAPOLIS, March 17, 2011 – Eli Lilly and Company (NYSE: LLY) announced today that patients should not use the alcohol prep pads made by the Triad Group that are contained in the black starter kits for Forteo® [teriparatide (rDNA origin) injection] in the United States. The Triad Group is recalling the alcohol prep pads due [...]

McNeil Consumer Healthcare Announces Voluntary Recall of Certain OTC Infants’ and Children’s Products

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Fort Washington, PA (April 30, 2010) – McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., in consultation with the U.S. Food and Drug Administration (FDA), is voluntarily recalling all lots that have not yet expired of certain over-the-counter (OTC) Children’s and Infants’ liquid products manufactured in the United States and distributed in the United States, Canada, [...]

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