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.
1,488 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Curtis International recalled Frigidaire-brand minifridges on July 24, 2025. The recall affects models EFMIS129, EFMIS137, EFMIS149, and EFMIS175, due to fire and burn hazards. More than $700,000 in property damage has been reported.
Innovative Designs recalled Minecraft Light-Up Slap Ruler Bracelets on July 24 due to a serious ingestion hazard. The product's battery compartment can be easily opened by children, exposing button cell batteries. This poses a risk of serious injury or death.
Minongad recalled LED gloves model ST01 on July 24, 2025, due to a serious battery ingestion risk. The gloves contain lithium coin batteries that can be accessed by children, posing a high danger of serious injury or death. Consumers should stop using the gloves and return them for a full refund.
Aiho recalled five-drawer dressers on July 24, 2025, due to tip-over and entrapment hazards. The dressers, model number AP23-W, do not meet safety standards set by the STURDY Act. Consumers should stop using the product if it is not anchored to a wall.
Creekwood Naturals recalled Gum Spirits of Turpentine bottles due to non-compliance with child-resistant packaging standards. The recall affects bottles sold since July 2025. Consumers should secure this product away from children immediately.
Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes on July 22, 2025. The recall stems from a lack of assurance of sterility, posing a high risk to users. Consumers and healthcare providers must stop using these towelettes immediately.
Middlefield Original Cheese Cooperative recalled 640 pounds of cheese on July 21, 2025. The recall affects Monterey Jack and Farmers Cheese due to potential Listeria monocytogenes contamination. The products were distributed in Kentucky, Ohio, and Pennsylvania.
Ascend Laboratories recalled 8,568 bottles of Amlodipine and Olmesartan Medoxomil Tablets on July 21, 2025. The recall follows reports of low dissolution results, impacting the drug's effectiveness. Consumers should stop using the product and seek guidance immediately.
Middlefield Original Cheese Co-op recalled 246.5 pounds of 100% Grass-Fed Pepper Jack Cheese on July 21, 2025. The cheese may be contaminated with Listeria monocytogenes, which can cause serious illness. Consumers should not eat this product and seek a refund.
Merck Sharp & Dohme LLC recalled 51,320 cartons of Belsomra (suvorexant) tablets on July 21, 2025. The recall stems from a failure in dissolution specifications that could delay drug release. Consumers should stop using the product immediately and consult healthcare providers for guidance.
AUM Pharmaceuticals recalled 50,000 cartons of Quick Touch Alcohol Prep Pads on July 21, 2025, due to cGMP deviations. The recall affects sterile pads containing 70% isopropyl alcohol. Consumers should stop using the product immediately and contact the manufacturer.
DJO Surgical recalled 439 AltiVate Reverse Glenoid Trays on July 18, 2025, due to potential reamer malfunction. The reamer may kick or bind during use, posing a serious risk to patients. Healthcare providers should stop using the device immediately and follow the recall instructions.
DJO Surgical recalled 447 units of the Altivate Reverse Wedge Glenoid Reamer Sleeve on July 18, 2025. The recall follows reports that the device may kick or bind during use, presenting a serious hazard to patients. Healthcare providers and patients should discontinue use immediately and follow the manufacturer's instructions.
DJO Surgical recalled 927 units of the Altivate Reverse Wedge Glenoid Reamer Head on July 18, 2025. The recall follows reports that the device may kick or bind up during use. Healthcare providers and patients must stop using the product immediately.
DJO Surgical recalled 907 units of the Altivate Reverse Wedge Glenoid Reamer on July 18, 2025, due to a kickback risk during use. The recall affects healthcare providers and patients nationwide across 25 states. This Class II recall warns of potential binding issues that could lead to serious injury.
Primark recalled DTR Stitch Scented Highlighters on July 17, 2025, due to phthalate exposure. The highlighters, resembling slushie containers, pose a health risk to children. Consumers should stop using them immediately and seek a refund.
C.R. Bard Inc issued a recall for 4,300 Foley catheter trays on July 17, 2025. Incorrect inserts lead to potential allergic reactions and infection risk. Healthcare providers and patients must stop using the device immediately.
VIVI recalled lithium-ion batteries for e-bikes on July 17, 2025. The batteries can overheat, posing fire and burn hazards. Consumers must stop using the affected e-bikes immediately.
DermaRite Industries recalled 6,973 cartridges of KleenFoam Antimicrobial Foam Soap on July 17, 2025. The product contains a harmful bacterial contamination, Burkholderia cepacia. Consumers should stop using the soap immediately and seek guidance from healthcare providers.
Deale International recalled CasaClean Handheld Steamers on July 17, 2025, due to a burn injury hazard. The recall affects model DF-958, sold at HSN from November 2024 through April 2025 for about $40. Users should stop using the product immediately and follow refund instructions.