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.
Immediate attention
Agrish recalled adult portable bed rails on January 8, 2026. The recall affects models 2512, 2513, and 2516 due to an entrapment hazard. Consumers should stop using the product and seek a full refund.
Kori Gey recalled water elf toy kits on January 8, 2026, due to a severe risk of battery ingestion. The toy kits can expose children to dangerous button cell batteries. Consumers should stop using the kits immediately and seek a refund.
Marcus Adler Glove recalled Julie and Judah pajama pants and shorts on January 8, 2026. The products violate mandatory flammability standards for children's sleepwear. Consumers should immediately stop using these items and seek a refund.
NFSVLB recalled baby bath seats on January 8, 2026, due to a drowning hazard. The recall affects the model number ZY2025, which can tip over and entrap children. Consumers must stop using the seats immediately and seek a refund.
Lterfear recalled the Multifunction Pounding Game model D888 on January 8, 2026. The toy poses a serious ingestion hazard due to high-powered magnets that can detach. Consumers should stop using the toy immediately and seek a refund.
Island Crab Corporation recalled 23 units of Smoked Grouper Dip on January 8, 2026. The product contains undeclared allergens including milk, eggs, and sodium metabisulfite. Consumers should not consume this product and seek a refund.
Outside The Breadbox recalled 4,497 units of bread crumbs on January 8, 2026. The product contains undeclared allergens: egg and milk. Consumers in CO, MS, ND, NE, RI, TN, TX, and WI should not consume the product.
Medline Industries recalled 2,020 dialysis kits on January 8, 2026, due to defective silicone seals. The seals may dome or tear, leading to fluid leaks and contamination. Patients and healthcare providers should stop using these kits immediately.
Medline Industries recalled 9,720 convenience kits on January 7, 2026, due to sterilization calibration issues. The affected products may not meet sterility assurance levels. Patients and healthcare providers should stop using these kits immediately.
Devices which did not undergo thermoforming could deform and lose performance.