Tristar Equine Marketing, LLC is recalling all lots of Gastrotec down to the consumer level. Gastrotec was previously marketed by Tristar as an OTC drug for use in horses, and contains a combination of Omeprazole and Misoprostol. This recall has been initiated due to information from the FDA that Gastrotec must have an approved new animal drug application to be legally marketed in the United States. Gastrotec is not approved by the FDA. As a consequence, Tristar has ceased all production and sales of Gastrotec and is recalling the product.
The Oregon Board of Pharmacy (OBP) is proposing an administrative rule that would allow it to inspect veterinary practices and other drug outlets to ensure that medications are safely handled and stored.
Natura Pet Products has recalled certain dry cat and dry ferret food lots produced in its Fremont, Nebraska facility. Due to a formulation error, these products contain insufficient levels of vitamins and excess minerals.
Veterinary professionals, like most caregivers, tend to be naturally compassionate people, but sometimes caring too much can hurt. It’s hard to remain emotionally unaffected by the trauma your patients (and their owners) are experiencing. Seeing and caring for severely injured and acutely ill animals day after day – some of which are untreatable, while others might be medically treatable but still need to be euthanized because their owners cannot afford treatment – takes its toll.
New guidelines for how to manage pets that have been potentially exposed to Ebola have been developed by veterinary and public health experts from the AVMA, CDC, USDA and other organizations.
Oregon Compounding Centers, Inc., dba Creative Compounds, is voluntarily recalling certain unexpired human and veterinary sterile products to the consumer level due to lack of sterility assurance. The recalled veterinary products include: Apomorphine HCL 3mg/ml injectable, Cyclosporine-E Plus 2% Ophthalmic, and Polysulf Glucosamin Glycan 10% injectable.
While not having your own DEA license may save an associate or the practice the cost of the license fee, there are several reasons why this is not advisable.
With three months left in the calendar year, 2014 already has been significant for the welfare of animals, and for Oregon in particular. Following is a look at recent developments as well as highlights from several court cases that have bearing on the state’s approach to animal welfare.
Bravo of Manchester, CT is recalling select lots of Bravo Turkey and Chicken pet foods for dogs and cats because they have the potential to be contaminated with Salmonella. Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.
Concerned about the diversion of hydrocodone combination products (HCPs) and the potential for abuse, the Drug Enforcement Administration (DEA) has rescheduled all hydrocodone combination products as Schedule II, effective October 6, 2014. The new scheduling impacts all HCPs, including liquids such as Tussionex, Hycodan and all generic equivalent products. Single-entity hydrocodone has always been a C-II drug.
Salmon poisoning disease is a potentially fatal condition seen in dogs who have ingested certain types of raw fish found in the Pacific Northwest from San Francisco to the coast of Alaska. It is most prevalent from northern California to the Puget Sound. It is also seen inland along the rivers of fish migration.
Congratulations to Midnight and owner Peter Wong! As the winners of our Oregon State Fair Wellness Exam contest, they won $100 towards a preventive health exam, as well as a complete bloodwork panel (courtesy of Idexx).
The Oregon Veterinary Medical Examining Board has proposed two rule changes related to background checks for licensees and CVT licensure reciprocity. Comments on these two proposed rules are due by September, 22, 2014.
At its July meeting, the Oregon Veterinary Medical Examining Board approved moving ahead to require that veterinarians and veterinary technicians undergo a criminal background check before licensure is granted.
The Drug Enforcement Administration (DEA) has published its decision to add Tramadol as a controlled substance. The rule becomes effective August 18 of this year.
Cargill’s animal nutrition business today announced a voluntary recall of its Nutrena NatureWise meatbird feed due to excess levels of sodium.
Learn how to foreclose on liens involving animals left at your clinic after services were rendered.
PGG/HSC Feed Company, LLC has recalled 50 pound packages of its Champion Lamb Texturized B30 product due to higher than allowable copper levels. The product was manufactured in February 2014 and carries the UPC code UPC-748252483805 located in the bottom left corner of a white label attached to a Payback bag with a photo of a lamb.
Hill’s Pet Nutrition, Inc. of Topeka, KS is voluntarily recalling 62 bags of Science Diet® Adult Small & Toy Breed™ dry dog food as they have the potential to be contaminated with Salmonella. The suspect product, part of a single production run, was distributed to 17 veterinary clinic and pet store customers in California, Hawaii and Nevada between April 24 and May 13, 2014.
Pet Center, Inc of Los Angeles, CA is voluntarily recalling its 3 oz. bag of Lamb Crunchy’s dog treats (LAM-003) (UPC# 727348200038) with date code 122015, product of USA, because it has the potential to be contaminated with Salmonella.
Bravo is recalling select lots and product(s) of Bravo Pet Food because they have the potential to be contaminated with Listeria monocytogenes.
Oregon Administrative Rules require veterinarians to report certain diseases to the Oregon Department of Agriculture.
Porcine Epidemic Diarrhea virus (PEDv) disease has been added to the reportable disease list in Oregon. The PEDv is a highly contagious coronavirus that affects swine, causing diarrhea and vomiting, and death of 50-100 percent of infected piglets. Adult pigs can become infected but generally do not have mortality.
Hospira has recalled to the user level one lot of 0.25% Marcaine™ (Bupivacaine HCl Injection, USP), 10 mL, Single-dose Vial – Preservative Free (NDC 0409-1559-10), Lot 34-440-DD. The recall is due to a confirmed customer report of discolored solution with visible particles embedded in the glass as well as discolored solution.
Hospira, Inc. has recalled one lot of 1% Lidocaine HCI Injection, USP to the user level due to a confirmed customer report of orange and black particulate within the solution and embedded within the glass vial. Hospira has identified the particulate as iron oxide. Risk factors associated with the particulate include the potential for particulate to be injected and/or a delay in therapy.