Dietary Supplement and Medical Device Recalls
Insulet Corporation recalls Omnipod Alternate controller enabled insulin infusion pump
Insulet Initiates Voluntary Medical Device Correction for Certain Omnipod® 5 Pods in the U.S.
ACTON, Mass.--(BUSINESS WIRE)-- Insulet Corporation (NASDAQ: PODD) (“Insulet” or the “Company”) today initiated a voluntary Medical Device Correction for specific lots of Omnipod® 5 Pods after identifying a manufacturing issue through its ongoing product monitoring. This action applies to specific identified lots distributed in the United States, and all other Omnipod® 5 Pods and Omnipod® products remain safe to use.
Insulet identifed that certain Pods from specific lots may have a small tear in the internal tubing that delivers insulin. If this occurs, insulin may leak inside the Pod instead of being fully infused into the body as intended.
If insulin is not delivered properly, users may experience high blood glucose levels due to under-delivery of insulin. In the most severe cases, prolonged and persistent high blood glucose levels can lead to diabetic ketoacidosis (DKA), a serious medical condition that requires prompt medical treatment.
Primal Supplements Group LLC recalls Primal Herbs Dietary supplement
Primal Herbs Issues Voluntary Nationwide Recall of Primal Herbs Volume Due to Undeclared Sildenafil
FOR IMMEDIATE RELEASE - February 27 2026 — Albuquerque, New Mexico, Primal Supplements Group LLC is voluntarily recalling all orders of Primal Herbs Volume placed between July 2 and September 19, 2025, because FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label.
Sildenafil is the active ingredient in the FDA-approved prescription drug Viagra, used to treat erectile dysfunction. FDA approval of Viagra is restricted to use under the supervision of a licensed health care professional. This undeclared ingredient may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. People with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates.
Food and Beverage Recalls
Lidl US recalls Favorina Chocolate Ladybugs - German-Style Nougat Candy
ARLINGTON, VA – Lidl US is recalling all lots of their Favorina Chocolate Ladybugs - German-Style Nougat 3.52 oz box UPC 20304492 due to undeclared hazelnut allergen. People who have allergies to hazelnuts run the risk of serious or life-threatening allergic reactions if they consume these products.
The products were distributed between 01/28/2026 - 03/11/2026. The product was distributed to all Lidl US store locations in Delaware, District of Columbia, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, and Virginia.
No illnesses have been reported to date.
Pure Vitamins and Natural Supplements, LLC recalls Boner Bear, Red Bull and Blue Bull Honey dietary supplement
March 14, 2026- Pure Vitamins and Natural Supplements, LLC of Tampa, FL is voluntarily recalling Boner Bear Honey, Red Bull Extreme and Blue Bull Extreme. FDA laboratory analysis confirmed that Boner Bear Honey, contains sildenafil and tadalafil and Red Bull Extreme and Blue Bull Extreme contains sildenafil not listed on the product label.
Sildenafil and tadalafil are the active ingredients in the FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional. These undeclared ingredients may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. People with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates.
These products are marketed as sexual enhancement honey products and are packaged in plastic tubes of single servings.
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