Animal and Veterinary Recalls
Vet Plus, Inc. recalls FI Supplements
Fi Recalls Supplements for Dogs Because of Possible Salmonella Contamination
Fi, of New York, NY, is recalling the supplements for dogs listed below because they have the potential to be contaminated with Salmonella due to an ingredient supplied to Fi’s manufacturer. The manufacturer has suspended production while it investigates. Fi is promptly notifying all affected customers out of an abundance of caution.
Salmonella can affect the animals eating the product, and there is a potential risk to humans from handling contaminated products or from animal waste after the animals have ingested the product. This risk is greater if they have not thoroughly washed their hands after having had contact with the products, surfaces exposed to these products, or animal waste.
Drug and Dietary Supplements Recalls
American Regent, Inc. recalls American Regent, Inc. Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial
FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility. The firm’s investigation also revealed the presence of particulate matter identified as Nylon, Cellulosic, Acrylic, Polyethylene and Glass.
Risk Statement: Intravenous administration of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) containing 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. Additionally, cracked vials can compromise the integrity of the container resulting in loss of sterility and potential contamination which can pose a serious risk for patients. To date, American Regent has not received any reports of adverse events related to this recall.
BMC Medical Co., Ltd. recalls BMC Luna G3 APAP (Model LG3600)
On July 15, 2026, BMC Medical Co., Ltd. (BMC), Beijing, China, retrospectively reported to the US Food and Drug Administration (FDA) a recall of 20,160 Luna G3 APAP (Model LG3600) devices distributed in the United States due to firmware defect. This corrective action was not reported to customers. On August 19, 2026, the FDA classified this retrospective recall as a Class I recall (FDA Recall Number: Z-2979-2026).
BMC has identified that firmware version, G3-2.00.76 installed on these Luna G3 APAP (Model LG3600) devices contained a firmware defect. BMC conducted a firmware upgrade of these devices to version G3-2.00.77 for 20,160 affected devices at the U.S. importer’s warehouse from October through December 2024. After reporting the retrospective recall, BMC discovered that potentially up to 196 units did not receive the upgrade and identified that these devices may still contain firmware version G3-2.00.76.
SUPPLX.com realls Business Pill, Branch Manager for Men dietary supplements marketed for male sexual enhancement
Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.
Yohimbine is a plant-derived alkaloid formulated for use as a prescription medication, generally as a treatment for erectile dysfunction. It has also been studied for use to promote blood flow and support athletic performance. FDA found dangerously high levels of yohimbine in the recalled products. Yohimbine can cause severe hypertension, tachycardia, and possibly cardiac arrhythmia and myocardial infarction (heart attacks), especially if the consumer is taking other stimulants such as caffeine or ephedra-containing products or prescription drugs used to treat ADHD. Severe gastrointestinal distress, including nausea, vomiting, diarrhea and stomach pain are typical side effects of high doses. It can also cause acute neurologic and psychiatric effects, including anxiety, insomnia, mania, psychosis in schizophrenic patients, drowsiness, disorientation, tremors and seizures. Death has been reported in cases of severe overdose.
Food and Beverage Recalls
Foods Alive Inc. recalls Foods Alive Inc. Moringa Leaf Powder
Foods Alive Recalls Organic Moringa Leaf Powder Because of Possible Health Risk
Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to 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 organic moringa leaf powder was distributed nationwide in retail stores and through online sellers including but not limited to www.foodsalive.com
FreshPoint Central Florida, Inc. recalls Created Fresh! Cranberry Chicken Salad Wedge Sandwich
September 4, 2026 Orlando, FL– FreshPoint of Orlando, FL., is issuing a voluntary recall of 1,093 units of specific lots of Cranberry Chicken Salad Wedge sandwiches due to an improperly declared allergen (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 recalled sandwiches were distributed from August 19th, 2026, to September 3rd, 2026, to a single convenience store customer in the states of Georgia and Florida.
The recalled sandwiches are packaged in transparent plastic packages and the Use by Date is printed on the clear plastic container.
Frutas y Hortalizas del Sur S.A. recalls Great Value Organic Triple Berry Blend
September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145).
E. coli O145 is a Shiga toxin-producing E. coli (STEC) that can cause illness characterized by severe stomach cramps, diarrhea (which may be bloody), and vomiting. While most healthy individuals recover within a week, some infections may result in a serious complication known as hemolytic uremic syndrome (HUS), particularly in young children, older adults, and individuals with weakened immune systems.
Made Fresh Salads Inc. recalls Made Fresh Salads, Northside Ready to Eat Deli Style Salads and cream cheese
Made Fresh Salads Inc. of Bay Shore, NY is recalling all Ready to Eat Deli Style Salads and cream cheese, because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
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