2,756 recalls tagged with “immediate action”.
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.
PNW Components recalled its Loam Pedal Gen 2 on January 9, 2026, after reports of axle cracks. The defect can cause pedals to detach, posing a fall risk. Customers should stop using the pedals immediately and seek replacements.
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.
Devices which did not undergo thermoforming could deform and lose performance.
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation recalled 1,474 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to improper thermoforming. Healthcare providers and patients must stop using these instruments immediately.
Devices which did not undergo thermoforming could deform and lose performance.