Drug and Dietary Supplement Recalls
Leader Formulas, LLC. recalls RAPTURE Preworkout Dietary Supplement Powder
Leader Formulas, LLC. of Tomball, TX, is voluntarily recalling one (1) lot of RAPTURE Pre workout, a dietary supplement powder because it was found to contain 1,3-Dimethylamylamine (DMAA) and sold at the consumer level. Using DMAA can result in elevated blood pressure and could lead to cardiovascular problems, including heart attack, shortness of breath and tightening of the chest.
The product is used as a dietary supplement and is packaged in 450g round plastic containers with red and black lettering and a rhinoceros print seal on top of the container. The affected RAPTURE Preworkout lots include the following lot number (260327-4). The product can be identified in the article linked above.
Pacific Health Sciences recalls Babies' Magic Tea brand Baby Sleep Gripe Water 4 oz bottle
Pacific Health Sciences is voluntarily recalling one lot of Babies' Magic Tea brand Baby Sleep Gripe Water dietary supplement.
Product Information
Product: Babies' Magic Tea brand Baby Sleep Gripe Water
Lot Number: 25122bw
Best Before: 12/2028
Package: 4 fl oz (approximately 118 mL) amber bottle inside a blue cardboard box. The lot number appears on the bottom of the box and on a side panel of the bottle. An oral syringe is included in the box.
Reason for Recall
FDA testing of this lot identified ethanol, methanol, and isopropanol that were not declared on the product label. Measured levels were approximately 8.3% ethanol, 0.35% methanol, and 0.48% isopropanol. These substances were not listed on the label. Their presence may pose a risk depending on the amount consumed and the age and body weight of the person using the product.
Par Health recalls Par Pharmaceutical Brevital Sodium 500 mg/vial for Injection
FOR IMMEDIATE RELEASE - ROCHESTER, MI– October 8, 2026 –Par Health is voluntarily recalling two lots of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) to the hospital level. The product is being recalled due to the presence of particulate matter identified as cellulose.
Administration of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for 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 inflammation of the walls of veins, which may lead to clotting. To date, Par Health has not received any reports of adverse events related to this recall.
Food and Beverage Recalls
Eden Brothers LLC recalls EDEN BROTHERS Broccoli Seeds - Calabrese
Eden Brothers Recalls Calabrese Broccoli Seeds Due to Possible Salmonella Contamination
Arden, NC – October 7th 2026 – Eden Brothers LLC is recalling Calabrese Broccoli Seeds in Packet, 1 Ounce and 1 Pound sizes (Eden Brothers lots 1022067 and 1022068; supplier lot W4105) because we were informed by our supplier that they may be contaminated with Salmonella.
Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. In rare cases, a Salmonella infection can enter the bloodstream and cause more severe illness.
Gardeners Basics recalls Gardeners Basics Broccoli Sprouting Seeds
October 8, 2026, Gardeners Basics of Spanish Fork, Utah, is recalling one-pound bags of broccoli sprouting seeds 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 product was distributed nationwide in the United States through online sales and shipped directly to consumers.
Krasnyi Oktyabr Inc. recalls Starfish Seafood Cold Smoked Salmon, Halibut, and Trout
Krasnyi Oktyabr Inc. Recalls Starfish Seafood Trio Because of Possible Health Risk
Krasnyi Oktyabr Inc. of Brooklyn, New York, is voluntarily recalling Starfish Seafood Trio – Cold Smoked Salmon, Halibut, and Trout, 8 oz (227 g) packages, because the product has 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.
The recalled product was distributed in New York, Florida, Georgia, Massachusetts, North Carolina, and South Carolina.
Oliva LLC. recalls Riad's Oliva to Go Baba Ghanouj, Spicy Baba Ghanouj, and Hummus
Oliva LLC Issues Allergy Alert on Undeclared Sesame in Baba Ghanouj, Spicy Baba Ghanouj, and Hummus
Oliva LLC of Bethlehem, CT is recalling approximately 250 units of Riad’s Oliva to Go Baba Ghanouj, Spicy Baba Ghanouj, and Hummus, because it may contain undeclared sesame. People who have an allergy or severe sensitivity to sesame run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled products were distributed to gourmet shops and farm markets in Litchfield County CT and Great Barrington, MA areas.
The recalled products are packaged in clear plastic square containers, with a white and green labeling, and best by stamped on side of label.
Medical Device Recalls
Nova Biomedical recalls Nova Biomedical StatStrip Glucose Hospital Meter System
Nova Biomedical® Announces Global Medical Device Correction for StatStrip® Glucose Hospital Meter
WALTHAM, Mass., October 5, 2026 – Nova Biomedical initiated a global Medical Device Correction on July 24, 2026, for the StatStrip® Glucose Hospital Meter System due to a software issue that may cause a glucose result to be associated with the wrong patient. When a patient ID barcode is scanned, prior patient information may remain on the meter screen, which if accepted, will lead to glucose result being assigned to the wrong patient’s medical record. If not recognized, healthcare providers may make clinical decisions based on another patient’s glucose result, potentially leading to delayed treatment, unnecessary treatment (including inappropriate insulin administration), and/or failure to treat the intended patient. The severity of harm depends on the patient’s actual glucose status and clinical condition.
Read Comments