American Regent is conducting a nationwide voluntary recall of Ammonium Molybdate Injection, USP (Molybdenum 250mcg/10mL) 10mL Single Dose Vial NDC 0517-6610-25, Lot # 9409, Exp. Date June 2011. This recall was initiated on April 26, 2011 to the User Level for Lot # 9409 only. No other lots of Ammonium Molybdate Injection, USP are subject to this recall.
Greenstone LLC announced a recall of medicines with lot number FI0510058-A on the label. Bottles labeled as Citalopram (used to treat depression) may contain Finasteride (used for the treatment of benign prostatic hyperplasia).
H&P industries, Inc., a manufacturer of over-the-counter products has initiated a voluntary product recall of all lots of Povidine Prep Pads manufactured by H&P Industries, Inc. but which are private labeled for many accounts.
The Food and Drug Administration’s Center for Veterinary Medicine (CVM) has become aware of a human drug recall for Phenobarbital tablets. Phenobarbital is prescribed by veterinarians as an extralabel use for treating seizures in animals.
American Regent Recalls Specific Lots of Dexamethasone Sodium Phosphate Injection Due to Particulates
American Regent is conducting a nationwide voluntary recall of specific Dexamethasone Sodium Phosphate Injections.
This recall was initiated because some of the vials of these lots may contain visible particulates. Potential adverse events after intravenous administration of solutions containing particulates may include disruption of blood flow within small blood vessels in the lung, localized inflammation (swelling and redness due to accumulation of inflammatory cells), and granuloma formation.
Jones Natural Chews Co of Rockford, IL is recalling 2705 boxes of Pig Ears because it has the potential to be contaminated with Salmonella.
At its July 23rd meeting, the OVMEB voted to rescind the proposed rule changes regarding exams and vaccines. The current rules remain in effect.
WellPet LLC has voluntarily recalled certain lots of Wellness® canned cat food due to the possibility that they contain less than adequate levels of thiamine (Vitamin B1).
American Regent is recalling one lot of Potassium Phosphates Injection, USP, 15 mM/5 mL Phosphorus; 22 mEq/5 mL Potassium, 5 mL Single Dose Vial.