Feline parasite solution gets FDA approvalNovember 26, 2019Merck Animal Health has received U.S. Food and Drug Administration (FDA) approval for an extended-duration topical solution that protects cats from fleas, ticks, and other parasites.
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Pig ear salmonellosis outbreak comes to a closeNovember 11, 2019Pig ear treats have officially been cleared for canine consumption, the U.S. Food and Drug Administration (FDA) says.
Hospira recalls bacteriostatic water for injectionSeptember 12, 2019Hospira, Inc., a Pfizer company, has issued a voluntary recall on one lot of sterile, nonpyrogenic preparation of water for injection due concerns over sterilization.
Human Salmonella cases linked to pig ears climb to 143August 30, 2019Cases of salmonellosis in humans connected to contact with pig ear treats continue to rise and the U.S. Food and Drug Administration (FDA) is advising pet owners to take precautions to avoid illness.
Third company issues pig ear recall over SalmonellaAugust 21, 2019A suspected connection between an outbreak of salmonellosis in humans and pig ear treats is forcing Dog Goods USA to issue a voluntary recall of some of its products.
Ellipse defibrillators, Agilia infusion pumps recalledAugust 15, 2019The U.S. Food and Drug Administration Center for Veterinary Medicine (FDA-CVM) has announced the voluntary recall two devices.
Raw pet food products test positive for Salmonella, ListeriaAugust 15, 2019Texas Tripe has recalled dozens of its raw pet food products after samples tested positive for Salmonella and/or Listeria monocytogenes (L. mono).
Pig ears linked to human cases of salmonellosisAugust 2, 2019Pet owners across 33 states are being advised to dispose all pig ear treats, as the products are believed to be linked to an ongoing outbreak of multidrug-resistant Salmonella infections in humans.
Horse deaths linked to compounded EPM drugsJuly 25, 2019An unapproved, compounded drug is believed to be linked to a recent string of horse deaths in the U.S.
Alaris infusion pump recalledJuly 23, 2019A manufacturing oversight has resulted in an FDA Class I recall of more than half a million infusion pumps across the U.S.
