State
72,907 recalls have nationwide distribution and so reach Florida. 12,818 additional recalls listed Florida specifically in their distribution scope.
Of the 12,818 recalls naming Florida we have scored against our rubric, 1,764 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,975 (23%) are Severe.
Which agencies issued them
These figures cover only the 12,818 recalls whose distribution notice names Florida specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Arrogantf spa drain covers sold on Amazon violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using them immediately and contact the importer for a refund.
About 2,355 CooCooBaby Classic and Deluxe Baby Loungers are being recalled for violating the mandatory standard for infant sleep products, posing a suffocation hazard.
Farber Specialty is recalling 2025-2026 HX620 and MCXCR emergency vehicles because the touchscreen may fail, preventing the activation of exterior lights and emergency equipment.
General Motors is recalling 2026–2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse when it encounters a person, potentially trapping them.
SHEIN Distribution Corporation is recalling about 160 Michley children's pajamas that violate the mandatory flammability standard for children's sleepwear, posing a burn injury or death risk. No injuries have been reported.
Piaggio is recalling 2026 Liberty 50 and 150 motorcycles because a circuit fault may cause headlights to turn off, increasing crash risk.
About 5,000 Arizer Solo III Intergalactic (Black) portable vaporizers are being recalled after four reports of the internal lithium-ion battery exploding or igniting.
Veseacky children's pajama sets are recalled due to burn hazards from violating mandatory safety standards for children's sleepwear. About 3,700 units were sold on Amazon from October 2020 through January 2026.
About 2,200 BABESIDE doll and stroller toy sets are being recalled because the small pacifier violates the small parts ban and the plush bear's eyes can detach.
About 1,060 Pyro Diablo "Diablo Rising" 9 Shots fireworks devices are being recalled because their pyrotechnic composition exceeds the federal limit.
About 3,840 Joolz Aer2 Car Seat Adapters are being recalled because they can fail to attach properly to the stroller, which may allow the car seat to fall.
Toyota Motor Engineering & Manufacturing is recalling 2026 Subaru Solterra vehicles due to a fault in the battery electronic control unit that may cause loss of drive power, increasing crash risk.
Beekeeper's Naturals Saline Nasal Spray with propolis and xylitol, 1 fl oz, is being recalled for microbial contamination of non-sterile products. 1,680 bottles are affected.
Gas-X Extra Strength simethicone 125 mg softgels are being recalled because of contamination with a diluted propylene glycol-based coolant leaked from a machine during packaging.
Doxorubicin Hydrochloride Liposome Injection, 50 mg/25 mL single-dose vials, is being recalled because of particulate matter identified as glass. 675 vials are affected.
HH Fresh Trading Corp. enoki mushrooms, 150 g, are being recalled after imported enoki mushrooms tested positive for Listeria monocytogenes. 120 cases are affected.
Whole Foods Market Kitchens Vegetarian Minestrone Soup, 24 oz, is being recalled because it contains undeclared shrimp. 562 cases, or 4,496 units, are affected.
Taro Cakes are being recalled because of an undeclared egg allergen. The action covers 300 units across all lot codes.
TNVitamins and Doctor's Pride moringa green superfood capsules are being recalled because the product may be contaminated with Salmonella. 13,000 bottles are affected.
The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.
CORFLO Safety PEG Kits, catalog number 30-6316, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 41 kits are affected.
Allia IGS 3 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. Nine units affected.
Plum Duo Infusion Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
SD LTM 64 PLUS EEG amplifier/recorders are being recalled because traces from different amplifiers in a multi-amplifier configuration may be displayed with a one-second shift.
MIC Safety PEG Kits with ENFit Connectors, 24 Fr PUSH OTW, catalog number 8170-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.