The US Food & Drug Administration (FDA) has recalled more than 6,000 promotional packs of M&M’s after identifying undeclared allergens in repackaged products distributed across 20 states. The recalled classic M&M’s were distributed in multiple promotional formats, including corporate and event branding such as Subaru, Adobe, Morgan Stanley, Best Western, Dropbox DocSend and Berkshire Hathaway Guard Insurance Companies. Read More –
Akkarco LLC Recalls Product Due to Possible Health Risk
Akkarco LLC of Lorton, Virginia, is voluntarily recalling Ashfiat Alharamain Energy Support because the product contains undeclared Tadalafil, an ingredient in FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE5) inhibitors. Products containing tadalafil cannot be marketed as dietary supplements. Ashfiat Alharamain Energy Support is an unapproved new drug for which safety and efficacy have not been established.
Nearly 85,000 bottles of Parodontax Active Gum Health Mouthwash are being recalled because some bottles may be missing or have incorrect lot numbers and/or expiration dates, according to the Food and Drug Administration.
Mays Chemical Company of Puerto Rico, located in Cataño, Puerto Rico, is recalling approximately 46,315 pounds of frozen, raw pork boneless loins that were not presented for import reinspection into the United States.
There’s an active recall on 22,896 bottles of cholesterol medication sold nationwide, according to the U.S. Food & Drug Administration (FDA).1 This is due to a chemical issue that may cause health concerns for consumers.
The prescription medication affected are 120-count bottles of Icosapent Ethyl manufactured by Softgel Healthcare and distributed by Zydus Pharmaceuticals. The medication is typically used alongside statins to lower high triglyceride levels and to reduce risk of serious cardiovascular events, including heart attacks. Read More –
If you take a daily greens supplement, check the label. Why Not Natural of Houston, Texas, is recalling its Why Not Natural Organic Moringa Green Superfood Capsules because they may be contaminated with Salmonella, according to the U.S. Food and Drug Administration (FDA). Read More –
An ongoing recall of more than 42,000 bottles of turmeric supplements has been given a Class II risk level, the Food and Drug Administration announced on Jan. 23. The supplements—Qunol Extra Strength Turmeric (1,000-milligram capsules)—were initially recalled in December 2025 for mold contamination. The FDA’s Class II level indicates that there’s a remote risk of serious adverse health consequences from ingesting the supplements. Read More –
Costco has issued a recall for a bakery item sold in 22 states. Packages of mini beignets filled with caramel actually contain beignets with a chocolate-hazelnut filling, the company warned customers. The labeling error resulted in an undeclared hazelnut allergen, posing the risk of life-threatening allergic reactions for people with hazelnut allergies or sensitivities. Read More –
More than 80,600 Keurig coffee pods have been recalled in three states, according to the Food and Drug Administration (FDA). McCafé Decaf K-Cups, the at-home McDonald’s coffee pods produced by Keurig Dr Pepper, were initially pulled from shelves in early December due to mislabelling—the product may actually contain caffeine. On Jan. 23, the FDA gave the recall the second-highest risk level, Class II, meaning the risk of serious adverse effects is low, but there is a chance of temporary or reversible effects. Read More –
A recall is underway for 1.5 million bottles of stain remover sold at major retailers nationwide, the Consumer Product Safety Commission (CPSC) announced Thursday. The products, sold under the brand Angry Orange, may contain bacteria, including Pseudomonas aeruginosa, which is found widely in soil and water. Healthy people are usually not affected by this pathogen, but those with weakened immune systems face the risk of a serious infection if they’re exposed. Read More –
Gerber’s Arrowroot Biscuits are being recalled.
Gerber has taken this step after their supplier issued a recall of its arrowroot flour. This batch of flour was found to potentially contain foreign materials, including soft plastic and paper pieces. Gerber has since terminated its relationship with this supplier. Arrowroot flour is a grain-free, gluten-free powder derived from the rhizomes of the tropical West Indian Arrowroot plant. Read More –
The U.S. Food and Drug Administration (FDA) has shared additional details about ongoing safety concerns with certain lots of Abbott’s FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors.
Back in November 2025, Abbott warned the public that some of its continuous glucose monitoring (CGM) sensors were providing incorrect low glucose warnings. At the time, the FDA was still investigating the issue.
