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Saturday, October 27, 2012

Recalled Product

Date Brand Name Product Description Reason/ Problem Company Details/ Photo
10/19/2012 Banana Boat and Ultra Defense   Continuous spray sun care products   Potential risk of product igniting on the skin if contact is made with a source of ignition before the product is completely dry Energizer Holdings Inc. Select to View Firm Press Release
10/06/2012 NECC   Methylprednisolone Acetate, Betamethasone, Bupivicaine, more   Sterility; linkage to meningitis outbreak New England Compounding Center (NECC) Select to View Firm Press Release
10/05/2012 Hospira, Inc.   Lactated Ringer’s and 5% Dextrose   Container Leak and mold contamination Hospira, Inc. Select to View Firm Press Release
09/20/2012 Watson   Hydrocodone Bitartrate and APAP Tablets   Tablets are thicker and darker than specification Watson Laboratories, Inc. Select to View Firm Press Release Select to View Image of Product Label
09/12/2012 ACTRA-Sx 500   Dietary Supplement   Unapproved new drug Body Basics, Inc. Select to View Firm Press Release Select to View Image of Product Label
09/10/2012 Qualitest   Hydrocodone Bitartrate & Acetaminophen Tablets   Tablets may exceed weight specification and could be super-potent for the ingredients Hydrocodon Bitartrate & Acetaminophen Qualitest Select to View Firm Press Release
09/04/2012 Sun Pharmaceutical Industries   Nimodipine Capsules, 30 mg   May contain crystals of nimodipine Sun Pharmaceutical Industries, Inc. Select to View Firm Press Release



Source:- http://www.fda.gov/Safety/Recalls/default.htm
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