State
72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Plunge Buddy is recalling DIY Sauna Heater Kits because electrical conductors within the kits can overheat. Twelve reports of overheating have been received, with no fires or injuries.
Sunnyyes LED mini lights are being recalled because the lithium coin batteries can be easily accessed by children, the remote battery compartment screw does not stay attached, and the packaging lacks required warnings.
Chrysler is recalling certain 2022–2026 Voyager and Pacifica vehicles because the right and left side curtain airbags may have insufficient pressure retention due to improperly sealed seams, increasing the risk of ejection and injury during a crash.
MPINOI adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and mattress, and the rails lack the required hazard warning labels.
Petzl America is recalling Nomic and Ergonomic ice climbing axes because the shaft can break at the handle during use. Twenty-six shaft breakages have been reported, with no injuries.
Nissan is recalling 2026 Leaf vehicles because internal damage in the high voltage battery may cause a short circuit, increasing the risk of a fire.
Bluegrass Ingredients Inc. is recalling Butter-Rich Powder (50 LB. bags) due to potential Salmonella contamination. The product was distributed to Florida, Illinois, and Maryland.
Bluegrass Ingredients Inc. is recalling Butter Powder (50 LB bags, Product Number BDF0006, Lot 6018) due to positive Salmonella contamination. The product was distributed to Florida, Illinois, and Maryland.
Volvo Trucks is recalling certain 2025-2026 VNL (4) vehicles because the service brake may take longer than expected to release, creating a crash risk and violating Federal Motor Vehicle Safety Standard 121.
Cardinal Health is recalling Webcol Alcohol Prep pads because of non-sterility, with microbial contamination identified as Paenibacillus phoenicis. The FDA has classified this recall as Class I.
Aston Martin is recalling certain 2025-2026 DBX and 2026 DBX S vehicles because the tire pressure monitoring system light may not illuminate to warn drivers of underinflated tires.
Abbott is recalling one lot of the ID NOW Influenza A & B 2 test after confirming the lot has a higher occurrence of invalid rates than stated in the Instructions for Use.
Howmedica Osteonics is recalling the MICS3 Angled Sagittal Saw Attachment because the external screws securing the cover to the saw housing may loosen and detach during use.
Elekta is recalling Leksell Gamma Knife radiosurgery systems, covering the Perfexion, Icon and Elekta Esprit models, due to an adapter not being properly aligned or locked in place.
Volkswagen is recalling certain 2025 Jetta and Taos vehicles because the instrument panel may fail to display warning lights or gauges. This fails FMVSS 101.
ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423657, because the drainable large pouch may leak due to a manufacturing issue.
ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423653, because the drainable large pouch may leak due to a manufacturing issue.
USDA FSIS issued a public health alert for raw Blackwing organic beef and pork products produced without federal inspection. Consumers are urged to discard or return these items.
Volvo Trucks is recalling certain 2025–2026 VNL (4) vehicles because the instrument panel may fail while driving, potentially hiding critical safety information like the speedometer and warning lights.
GE Medical Systems is recalling Centricity Universal Viewer software versions 6.0 through 6.0 SP10.4.1 because user login credentials may be exposed on the local client workstation.
Baxter is recalling the Welch Allyn Spot Vision Screener VS100 on software version 3.2.0.1 because the display screen may unintentionally flicker, which may induce photosensitive seizure activity.
GE Medical Systems is recalling Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 because user login credentials may be exposed on the local client workstation.
ASUKAR FOODS CORP is recalling TETAS Mireya Cherry Milkshake (Colita con Leche) popsicles because they contain undeclared soy lecithin, which may cause serious reactions in consumers with soy allergies.
ConvaTec is recalling two lots of the EsteemBody Drainable Pouch, REF 423643, because the drainable large pouch may leak due to a manufacturing issue.
Diagnostica Stago is recalling the STA Liatest D-Di kit after investigations confirmed a positive bias in D-dimer measurements throughout the entire analytical range.