State
73,576 recalls have nationwide distribution and so reach Florida. 12,867 additional recalls listed Florida specifically in their distribution scope.
Of the 12,867 recalls naming Florida we have scored against our rubric, 1,775 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,456 (27%) are Severe.
Which agencies issued them
These figures cover only the 12,867 recalls whose distribution notice names Florida specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Friedrich is recalling about 2,000 Kühl Q and S window air conditioners because a control board failure can cause fire and burn hazards.
LANCHEZ pressure washers are recalled because they lack a ground-fault circuit-interrupter and adequate power cord, posing risks of shock or electrocution.
Sauna360 is expanding a recall of Tylö Halmstad and Kiruna Hybrid Saunas because the benches can collapse, posing a fall hazard to users.
Jaguar Land Rover is recalling specific 2019-2024 models because a DC-DC converter malfunction can cause loss of drive power and lighting, increasing crash risk.
Sauna360 is recalling infrared and hybrid saunas because panels can short circuit and overheat, posing fire and burn risks.
Toyota is recalling 617 specific 2026 Lexus and Toyota models because front steering knuckles may crack, potentially causing a loss of steering control.
JKMAX is recalling about 195,000 heated blankets and heating pads because internal wires can overheat, posing fire and burn risks.
Regfear is recalling BedsPick mattresses because they violate mandatory flammability standards, posing a risk of serious injury or death from fire.
Hayward Industries is recalling 400,000 BTU Universal-HC Series pool heaters because they can produce high levels of carbon monoxide, posing a risk of serious injury or death.
Toyworld168 is recalling Rainbow Mystery Squishy Bun Toys because water beads inside can expand and cause choking or intestinal obstruction if swallowed.
Tongyang Cycling is recalling Basecamp bicycle helmets because they violate mandatory safety standards, posing a risk of serious head injury or death.
Esjay is recalling toddler busy board toys because red knobs can detach, posing a choking hazard to children under three.
Char-Broil is recalling about 10,605 Bistro Pro Electric Grills because a grounding wire can disconnect, posing an electric shock hazard. No injuries have been reported.
SHEIN is recalling Pull & Chew Montessori Teething Toys because the silicone strings violate safety standards and pose a choking risk. No injuries have been reported.
Melissa & Doug is recalling about 84,000 Lights & Sounds Fire Truck Activity Board toys sold at Target and Amazon because a fire hose port can detach, posing a choking risk.
B. Braun Medical Inc. is recalling 0.9% Sodium Chloride Injection due to the presence of particulate matter, including iron oxide and fibers.
Medical Action Industries is recalling Single Shot Epidural kits containing Sodium Chloride ampules due to potentially compromised sterility.
American Regent, Inc. is recalling 31,935 vials of Epinephrine Injection due to the presence of particulate matter and broken vials.
International Sprout Holdings is recalling 50 lb. bags of alfalfa due to potential E. coli and Salmonella contamination. The product was distributed to wholesale consignees in 16 states, Puerto Rico, and several international locations.
Rewaco is recalling 106 three-wheeled motorcycles because a rear shock absorber connection may loosen, potentially causing a loss of vehicle control.
Nipro Renal Solutions is recalling MedicaLyte Liquid Bicarbonate Concentrate due to high endotoxin levels. The product is used in hemodialysis.
Medical Action Industries is recalling Epidural/Pain TQC kits containing Sodium Chloride ampules due to potentially compromised sterility.
Nipro Renal Solutions is recalling Citric Complete Liquid Citric Acid Concentrate due to high endotoxin levels. The product was distributed in the US and internationally.
Baxter Healthcare is recalling 606 bags of Dextrose Injection, USP, 70% due to the presence of stainless steel particles in the solution.
Given Imaging is recalling Bravo CF capsule delivery devices because they may fail to attach to the esophagus or detach from the device, posing risks of aspiration and perforation.