Animal and Veterinary Recalls
Northwest Naturals recalls Northwest Naturals Chicken Recipe
Northwest Naturals of Portland, Oregon is voluntarily recalling 53 cases (1,272 lbs.) of Northwest Naturals Frozen Chicken Recipe (cat food 2 lbs. bag) and 19 cases (684 lbs.) of Northwest Naturals Frozen Raw Diet for Dogs Chicken Recipe (6 lbs. bag) in the two lots identified due to Salmonella and/or Listeria monocytogenes contamination. Salmonella and Listeria monocytogenes can affect animals eating contaminated pet products, and there is risk to people from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with contaminated pet products or any surfaces exposed to contaminated pet products and infected animals.
People infected with Salmonella should monitor themselves for the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping, and fever. Most people recover without treatment, but in some people, diarrhea may be so severe that they need to be hospitalized. In these patients, Salmonella infection may spread from the intestines to the blood stream and then to other body sites resulting in more serious ailments, including arterial infections, endocarditis, arthritis, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with contaminated pet products should contact their healthcare providers.
Revival Animal Health recalls Shelter’s Choice, Breeder’s Edge Feline Milk Replacers
Revival Animal Health of Orange City, IA is recalling Breeder’s Edge® and Shelter’s Choice® Feline Milk Replacers due to low, levels of potassium, copper, folic acid, choline and/or pyridoxine (vitamin B6).
Kittens, especially neonates, are a very vulnerable population: their organ systems are immature, they grow rapidly, and they are entirely dependent on their milk as a source of all nutrients. Deficiencies that might be subclinical in adult cats can be rapidly fatal or cause permanent developmental damage in kittens. Kittens fed milk replacer that is deficient in copper, potassium, vitamin B6, folic acid, and choline face compounding, multi-system risks, such as anemia, neurological dysfunction, liver failure, kidney damage, skeletal diseases, and cardiac compromise. Due to the rapid growth of young kittens, clinical signs may appear within days to a few weeks, and the deficiencies can be fatal or cause permanent organ damage if not recognized in time. Consumers who have kittens that have consumed any of the recalled products and are showing clinical signs should contact their veterinarian.
Drug and Dietary Supplements Recalls
Ana Salazar Modela Tu Cuerpo Inc. recalls Lipofit Extreme 2.0 Fat Burner Dietary Supplement
FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level. The Food and Drug Administration (FDA) laboratory analysis has found Lipofit Extreme Fat Burner 2.0 to be tainted with undeclared fluoxetine in the daytime (AM) tablets and undeclared 2,4-dinitrophenol (DNP) in the nighttime (PM) tablets. Fluoxetine is an active ingredient in an FDA-approved drug used to treat conditions including depression, bulimia and obsessive-compulsive disorder. 2,4-Dinitrophenol (DNP) is a toxic substance (commonly used as a pesticide, dye, wood preservative and herbicide) that is illegally marketed as a weight-loss product and is not approved by the FDA for any use. Products containing fluoxetine and DNP cannot be marketed as dietary supplements. Lipofit Extreme Fat Burner 2.0 is an unapproved new drug for which safety and efficacy have not been established and, therefore, subject to recall.
Baxter International Inc. recalls Baxter 0.9% Sodium Chloride Injection, USP, 500 mL VIAFLEX Plastic Container
FOR IMMEDIATE RELEASE – AUG. 25, 2026 – DEERFIELD, Ill., Baxter International Inc. (NYSE:BAX) is voluntarily recalling two lots of 0.9% Sodium Chloride Injection due to the potential presence of particulate matter identified as fiberglass in the solution.
Risk Statement: Intravenous administration of 0.9% Sodium Chloride Injection containing fiberglass particulate matter may lead to serious adverse health consequences. Particulate matter can cause blockage and clotting in blood vessels, which can cut off blood flow to vital organs, lead to a life-threatening blood clot in the lungs (pulmonary embolism) and cause permanent organ damage or death. Additionally, these particles may cause local vein irritation, inflammatory reaction, aggravation of preexisting infections, and allergic reactions. As of 8/25/2026, Baxter has not received any reports of adverse events related to this issue.
Baxter International Inc. recalls Baxter Anticoagulant Sodium Citrate Solution USP, 250 mL VIAFLEX Plastic Container
FOR IMMEDIATE RELEASE – AUG. 25, 2026 – DEERFIELD, Ill., Baxter International Inc. (NYSE:BAX) is voluntarily recalling one lot of Anticoagulant Sodium Citrate Solution due to the potential presence of particulate matter identified as fiberglass in the solution.
Risk Statement: Anticoagulant Sodium Citrate Solution is intended for use with automated apheresis devices. Administration of Anticoagulant Sodium Citrate containing particulate matter may lead to adverse health consequences, the extent and severity of harm depend on the size, number, morphology and composition of the foreign material. In the absence of in-line filtration, these particles may cause local vein irritation, inflammatory or hypersensitivity reactions, and systemic embolization that could result in tissue or organ injury. As of 8/25/2026, Baxter has not received any reports of adverse events related to this issue.
B. Braun Medical Inc. recalls B. Braun 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container
FOR IMMEDIATE RELEASE – August 19, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron oxide.
Risk Statement: Administration of 0.9% Sodium Chloride Injection USP, found to contain particulate matter, has a reasonable probability of causing life-threatening adverse health consequences including pulmonary emboli (blockage in pulmonary blood vessels), occlusions of other blood vessels (which can lead to tissue death and possible organ damage), and/or phlebitis (inflammation of the walls of veins, which may lead to clotting). Systemically, foreign particles infused intravenously can cause systemic activation of the immune system, organ dysfunction, and hemolysis (breakdown of blood cells). To date there have been no reports of serious injury, death or other adverse events associated with this issue.
Food and Beverage Recalls
Crystal Temptations recalls Little Temptations Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.
Crystal Temptations Issues Allergy Alert on Undeclared Milk in Chocolatey Eyeballs
Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled product, sold under the Crystal Temptations brand, was distributed in Arizona, Texas, Virginia, Georgia, Massachusetts, North Carolina, Indiana, Nevada, California, New Jersey, Connecticut, Ohio, and Wyoming, through the following Retail stores; Marshalls, TJ Maxx, Homegoods, Sierra Trading post.
Everything Sprouts, LLC recalls Everything Sprouts Robust Radish Mix, 5oz Cups
Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.
Shiga toxin-producing Escherichia coli (STEC) are organisms that can cause serious and sometimes fatal infections in young children, elderly people, and others with weakened immune systems. Escherichia coli (STEC) O26:H11, E. coli O103:H25, and E. coli O168:H8 are three members of this group of Shiga toxin producing E. coli. STECs cause an acute diarrheal illness (often bloody diarrhea) within a few days of ingestion of the bacteria. Most people recover within a week. However, a subset of infected individuals (especially children < 5 years of age, the elderly, and immunocompromised individuals) may develop hemolytic uremic syndrome (HUS), a severe illness characterized by hemolytic anemia (red cell breakdown), thrombocytopenia (low platelet count) and renal failure. HUS can lead to death.
Jaime’s Foods ATX recalls Jaime’s Spanish Village Jalapeno Ranch Dressing
Jaime’s Foods ATX of Austin, TEXAS is recalling Jaime’s Spanish Village Jalapeno Ranch because it contains undeclared eggs. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume this product.
The product was sold at Central Market retail stores in Texas and local independent retailers in Austin, Texas beginning on April 3, 2026.
The recalled Jaime’s Spanish Village Jalapeno Ranch dressing is packed in 16 oz (45.5g) glass jars with UPC #199284564923. Recalled lot numbers include the following: 69, 86, 108, 113, 116, and 121. The lot code can be found stamped on the bottom of the jar.
No illnesses have been reported to date.
LMSI LLC recalls Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml
Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.
The recalled products were available for sale from August 31, 2025, to August 27, 2026, at the following locations:
Montgomery Store & Infusion Kitchen: 8210 Market Place Ln., Cincinnati, OH 45242
Findlay Market: 1801 Race St., Cincinnati, OH 45202
Online sales directly from www.kofinasoliveoil.com
Panorama Produce recalls Martina Mangoes
Panorama Produce Recalls Mangoes Due to Possible Salmonella Contamination
MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
The recalled product was distributed in the following states beginning on August 10 through August 21, 2026: CT, NY, NJ, and PA, and sold in select Walmart stores.
The recalled mangoes are packaged in a Martina-branded case. The individual mangoes can be identified by a light blue sticker with the label Agrofepac, Produce of Mexico, and a PLU number of 4584 and UPC # 07503061948050.
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