Verdict . News

•Recall affects Chocolate Cherry and Peanut Butter Chocolate Chip Junebars with batch labels L1300 or L1301

1w ago•4 min read

FDA Issues Allergy Alert for Junebars with Undeclared Milk and Soy

Juniper Granola, LLC of Rochester, NY has issued a voluntary recall of Chocolate Cherry and Peanut Butter Chocolate Chip Junebars containing undeclared milk and soy allergens. The recall affects products with batch labels L1300 or L1301, posing serious health risks to consumers with allergies.

•Undeclared milk and soy allergens pose serious health risks to consumers with allergies or sensitivities

•Prime Food Processing LLC voluntarily recalled 80 cases of dried croaker fish due to inadequate evisceration

FDA Issues Safety Warning for Improperly Processed Dried Croaker Fish

Prime Food Processing LLC has voluntarily recalled 80 cases of dried croaker fish after the FDA determined the products were not adequately eviscerated as required by federal regulations. The improperly processed fish may retain internal organs that could harbor harmful bacteria or toxins, posing potential health risks to consumers.

•FDA regulations require proper removal of internal organs to prevent bacterial contamination and toxin buildup

•Prime Food Processing LLC voluntarily recalled dried croaker fish for failing to meet FDA evisceration standards

Brooklyn Food Company Recalls Dried Fish Over FDA Safety Violations

Prime Food Processing LLC of Brooklyn voluntarily recalled dried croaker fish products after failing to meet FDA evisceration requirements. The recall highlights potential health risks from improperly processed fish products.

•Improperly eviscerated fish poses health risks including bacterial contamination and potential allergen exposure

•Why Not Natural voluntarily recalled Organic Moringa Green Superfood products due to Salmonella contamination risk

Houston Company Recalls Moringa Superfood Over Salmonella Risk

Why Not Natural, a Houston-based company, has voluntarily recalled its Organic Moringa Green Superfood products due to potential Salmonella contamination that poses serious health risks to vulnerable populations.

•Salmonella can cause serious or fatal infections in children, elderly, and immunocompromised individuals

•Ashfiat Alharamain Energy Support contains undeclared Tadalafil, a prescription erectile dysfunction drug ingredient

FDA Issues Recall for Energy Supplement Containing Undeclared ED Drug

Akkarco LLC of Lorton, Virginia, voluntarily recalled its Ashfiat Alharamain Energy Support supplement after discovering it contains undeclared Tadalafil, an active ingredient in FDA-approved erectile dysfunction medications. The hidden pharmaceutical ingredient poses potential health risks to unsuspecting consumers.

•The hidden pharmaceutical ingredient violates federal regulations and poses serious health risks to consumers

•Gerber voluntarily recalled limited batches of Arrowroot Biscuits due to potential soft plastic and paper contamination

3w ago•4 min read

Gerber Recalls Arrowroot Biscuits Over Foreign Material Risk

Gerber Products Company voluntarily recalled limited batches of Arrowroot Biscuits on January 26, 2026, due to potential contamination with soft plastic and paper pieces from an arrowroot flour supplier. The FDA announced the recall as a precautionary measure to protect infant and toddler consumers.

•Contamination originated from an arrowroot flour supplier that initiated its own recall

•Navitas Organics voluntarily recalls 8oz Organic Chia Seeds due to potential Salmonella contamination

3w ago•4 min read

Navitas Organics Recalls Chia Seeds Over Salmonella Risk

Navitas Organics has voluntarily recalled select lots of its 8oz Organic Chia Seeds due to potential Salmonella contamination. The recall was initiated as a precautionary measure following contamination concerns at the company's supplier.

•Recall initiated as precautionary measure following contamination issues at company's supplier

•Olympus voluntarily expanded recall of ViziShot 2 FLEX needles after components ejected during medical procedures

Jan 16, 2026•4 min read

Olympus Expands Medical Device Recall After Components Eject During Use

Olympus Corporation expanded its voluntary recall of ViziShot 2 FLEX medical needles following reports of device components ejecting or detaching during procedures. The FDA announced the expanded recall action on January 16, 2026, raising patient safety concerns.

•The devices are used in diagnostic chest procedures to obtain tissue samples from lymph nodes

•All Live it Up Super Greens products with lot numbers starting with 'A' and stick packs are being recalled

Jan 15, 2026•4 min read

FDA Announces Recall of Live it Up Super Greens Over Salmonella Risk

Superfoods Inc., operating as Live it Up of New York, has issued a voluntary recall of all Live it Up Super Greens products due to potential Salmonella contamination. The recall affects products with lot numbers beginning with the letter 'A' and all stick pack versions.

•Potential Salmonella contamination poses serious health risks including severe illness