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.
Boss Pet Products Recalls Diggers Natural Treat Pig Ear Pet Treats: Possible Salmonella Contamination
Boss Pet Products, Inc. announced that it is recalling its Diggers Natural Treat Pig Ear pet treats because the products have the potential to be contaminated with Salmonella. Boss Pet has been notified by one of its suppliers, Keys Manufacturing Company, Inc., that a batch of Keys’ pig ear treats tested positive for Salmonella. These treats were shipped to Oregon, among other states.
Blackman Industries Recalls PrimeTime Pig Ears and KC Beefhide Pig Ears: Possible Salmonella Contamination
Blackman Industries, Inc. of Kansas City, KS is recalling all PrimeTime brand 2 ct. and 5 ct. Premium Pig Ears and all KC Beefhide brand 20 ct. Premium Pig Ears because they have the potential to be contaminated with Salmonella. These products were sold in Kansas, Missouri, Iowa, Nebraska and South Dakota.
The FDA’s Center for Veterinary Medicine is alerting pet owners to use caution with the use of an unapproved animal drug product, Douxo Seborrhea Shampoo (0.1% phytosphingosine), distributed by Sogeval Laboratories, Inc. of Coppell, Texas after recently receiving a report of the death of a woman associated with the use of the product on her dog.
Triad Group, a manufacturer of over-the-counter products has initiated a voluntary product recall involving all lots of Alcohol Prep Pads, Alcohol Swabs or Alcohol Swabsticks manufactured by Triad Group which may be included in a variety of other products labeled with other manufacturers' names.
Keys Manufacturing Company, Inc. of Paris, IL is recalling Pig Ears for Pet Treats because it has the potential to be contaminated with Salmonella.
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).
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.
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.