These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
3,494 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Petmate recalled Pet Zone Laser Pointer & LED Ball toys sold exclusively at Menards. The recall date is August 7, 2025. The products contain six preinstalled button cell batteries and pose an ingestion hazard if the battery compartment is breached. Consumers should stop using the recalled toys and contact Petmate for a full refund.
Glenmark Pharmaceuticals Inc. recalls 6,432 bottles of Carvedilol Tablets, USP, 12.5 mg, distributed nationwide in the United States. The recall concerns CGMP deviations and the presence of a nitrosamine impurity above the acceptable intake level. Consumers should stop taking the product and contact Glenmark for guidance.
Monica Vinader recalls select 14k yellow gold mini heart bracelets, necklaces and stud earrings due to high cadmium levels. The recalled jewelry was manufactured in October and November 2024. Consumers should stop wearing the jewelry immediately and contact Monica Vinader for a replacement or refund.
Wang Globalnet recalled 1,705 cases of frozen raw oyster halves sold at 27 retail locations in the Northeast and Southwest. The two lots, B250103 and B250114, are under recall for potential Norovirus contamination. Consumers should not consume these oysters and should contact Wang Globalnet for refunds or replacements.
Fieldsheer Apparel Technologies is recalling heated socks MWMS07, MWWS07 and MWMS05. The recall covers socks sold with two lithium-ion battery packs and a charging cable. Consumers should stop using the product and contact Fieldsheer for a refund or replacement.
Glenmark Pharmaceuticals recalls 4,800 bottles of Carvedilol 25 mg tablets distributed nationwide in the USA. The recall cites CGMP deviations and a nitrosamine impurity exceeding the Acceptable Intake Level. Consumers should stop using the product and contact Glenmark or their healthcare provider for guidance.
TEMI Toys recalled the TEMI Go Basketball toy sold on Amazon due to a choking hazard for children under three. The toy stands about 13 inches tall and 4 inches wide and includes three yellow balls. TEMI Toys is offering a full refund to consumers who stop using the product and contact the company.
Séfralls Minoxidil Hair Generation Serum, sold by Guangzhou Ariel Biotech, was recalled on August 7, 2025. The serum is packaged in amber dropper bottles with a white and gold dropper and a white, black and gold label. The packaging is not child-resistant, violating the Poison Prevention Packaging Act and creating a poisoning risk for children. Consumers should stop using the serum immediately and
Glenmark Pharmaceuticals Inc. recalls 44,328 bottles of Carvedilol tablets, 3.125 mg, distributed nationwide in the USA. The impurity N-nitroso carvedilol I exceeds the Acceptable Intake Level. Consumers should stop using the product and contact Glenmark for guidance.
AliExpress recalls LeymanKids children's two-piece pajama sets sold online. The recall stems from a violation of mandatory flammability standards for children's sleepwear. Consumers should stop using the pajamas immediately and pursue a full refund through AliExpress.
La Ligne recalls Enfant Bonne Nuit children’s pajamas after a burn hazard was identified. The recall covers La Ligne by La Ligne Enfant Bonne Nuit two-piece sets sold in various colors. Consumers should stop using the pajamas and pursue a full refund or store credit.
Deale International recalls Altafit AF28 smartwatches sold by HSN after reports of overheating charging pads. The recall cites a risk of serious burn injury and fire. Consumers should stop charging the watch immediately and contact Deale International for a free replacement.
The Candy Barn recalled 665 packages of its Chocolate Fudge on August 6, 2025. The product does not list egg in the allergen statement, posing a risk to those with egg allergies. Consumers should not consume the product and seek a refund.
The Candy Barn recalled 665 packages of English Toffee on August 6, 2025. The product contains undeclared pecans, posing a risk to those with tree nut allergies. Consumers should not eat the candy and should seek a refund or replacement.
The Candy Barn recalled 665 packages of Maple Nut Fudge on August 6, 2025. The product contains undeclared allergens: pecans and eggs. Consumers should not consume the fudge and seek refunds.
The Candy Barn recalled 665 packages of Chocolate Pecan Fudge on August 6, 2025. The product lacks proper allergen labeling for pecans and eggs, posing a high risk to consumers. The recall affects products distributed in Kalona, Iowa.
The Candy Barn recalled 665 packages of Chocolate Mint Fudge on August 6, 2025. The product lacks proper allergen labeling for egg, posing a risk to consumers. The fudge was distributed in Kalona, Iowa at two grocery locations.
The Candy Barn recalled 665 packages of Pecan Toffee Clusters on August 6, 2025. The recall stems from a labeling issue where pecans were not listed in the allergen statement. Consumers should not consume these products and seek refunds.
Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition PhytoForm Fruits & Greens Formula after FDA enforcement flagged unapproved drug claims and misbranding. The dietary supplement was distributed to 40+ states before the recall was issued on 2025-08-06 and remains active. Consumers should not consume the product and should seek refund or replacement from Hi-Tech Pharmaceuticals.
Hi-Tech Pharmaceuticals recalled 85,950 units of Pine Bark Supplements for unapproved drug claims and misbranding. The FDA enforcement notice lists Hi-Tech Pharmaceuticals, Inc. of Norcross, GA as the marketer. The recall cites unapproved drug claims and misbranding as the reason. Consumers should stop using the product and contact the company for refund or replacement information.