Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Maitys drinkware charms are recalled because they contain loose magnets that violate the mandatory magnet standard, posing an ingestion hazard to children. About 16,400 units are affected.
Iron-containing dietary supplements from eleven brands are recalled because their packaging is not child-resistant as required by the Poison Prevention Packaging Act. About 356,140 units are affected.
Besslly Halloween Pumpkin Carving Kits are recalled because children can easily access the button cell batteries in the included tea lights, posing an ingestion hazard. About 650 units are affected.
VEEKTOMX VT103 mini power banks are recalled because the lithium-ion battery can overheat and ignite. Three fires causing minor property damage have been reported; no injuries.
Akron Brass is recalling Enovation Controls PowerView 700 displays that may fail to power on or respond to touch, preventing the activation of emergency lights and equipment.
Prestige-branded Supernova and Typhoon butane torch lighters are recalled because they do not have the child-resistant mechanism required by the mandatory lighter standard. About 4,300 units are affected.
The Member's Mark 7-foot Pre-Lit Twinkling Buck is recalled because the current limiting resistor can overheat if the wires are connected incorrectly, posing a burn hazard. About 2,460 units are affected.
Chrysler is recalling 2026 Jeep Wrangler vehicles because insufficient child seat tether welds may reduce restraint effectiveness during a crash.
Male-to-male extension cords sold on Walmart.com are recalled because their exposed prongs can become energized when one end is plugged into a generator, posing an electrocution risk.
Chrysler is recalling 2025–2026 RAM 1500, 2500, 3500, 4500, and 5500 vehicles due to a software error that may cause the instrument panel display to fail, hiding critical safety information like gear selection and warning lights.
Happiness Light LED lights are recalled because their lithium coin batteries can be accessed easily by children, posing an ingestion hazard. About 2,800 units are affected.
Muscccm pool drain covers are recalled because they violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act, posing entrapment and drowning hazards.
ShymeryDirect LED lights are recalled because their lithium coin batteries can be accessed easily by children, posing an ingestion hazard. About 295 units are affected.
Chrysler is recalling certain 2026 Jeep Cherokee vehicles because the brake system control module may fail, causing loss of anti-lock brakes (ABS) and electronic stability control (ESC), which increases crash risk.
Intuitive Surgical is recalling da Vinci S and Si Double Fenestrated Grasper Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Burlington Medical is recalling protective caps made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
JFE Franchising Inc is recalling Dumpling Vegetable and Loaded Dumpling Vegetable products due to the presence of glass fragments. The products were distributed across multiple U.S. states.
Toyota is recalling specific Lexus RC, GS, and IS models because a failing fuel pump can cause the engine to stall, increasing crash risk.
Cardinal Health is recalling two lots of Monoject Tuberculin Syringes because the packaging identifies them as 1 mL Luer Lock tuberculin syringes but the contents are U-100 insulin syringes.
Quality Choice Eye Drops Irritation Relief, containing tetrahydrozoline HCl and zinc sulfate, are being recalled for lack of assurance of sterility. 182,424 bottles are affected.
Civco is recalling the eTRAX Needle Sensor 16G for Aurora trackers because an inspection and programming error may cause the needle tip position to be incorrectly identified on the user interface.
Burlington Medical is recalling protective vests because of the potential for attenuation degradation over time, decreasing the lifespan of the garment.
Medline is recalling Thoracic Robots kits, model DYNJ908777B, because they contain recalled Olympus biopsy valves where rubber fragments may detach from the valve slit.
Mentor is recalling Artoura Breast Tissue Expanders in the smooth ultra high profile range because the infusion sets may contain a dull or blunt needle tip.
Mentor is recalling the CPX 4 US Breast Tissue Expander with Suture Tabs, smooth low height 650 cc, because the infusion sets may contain a dull or blunt needle tip.