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.
Taro Pharmaceuticals is recalling Lidocaine Ointment 5% due to failed content uniformity specifications during stability testing.
Wilson-Cook Medical Inc. is recalling 121,241 units of Hemospray Endoscopic Hemostat due to issues with endoscope adherence and the inability to spray powder.
Straumann USA LLC is recalling 216 GM Helix Implants because the packaging identification does not match the actual implant dimensions.
Boston Scientific is recalling StoneSmart Connect Console power adapters that may fail electrical safety testing due to high grounding resistance.
Well Lead Medical Co. Ltd is recalling SunMed Tracheal Tubes because a 6Fr suction catheter could not pass through the samples smoothly.
Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product is distributed nationwide.
ICU Medical is recalling IV Non-Dedicated Gravity Administration Sets because black specks in the drip chamber may cause healthcare providers to delay therapy.
Embecta Medical II LLC is recalling pen needles labeled 'For Investigational Use Only' that were inadvertently distributed as commercially marketed devices.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide.
ICU Medical is recalling 107,800 oncology sets because drip chambers may contain black specks from the molding process, which could lead to product replacement and therapy delays.
Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product was distributed nationwide in the USA.
ICU Medical is recalling 28,550 oncology sets because drip chambers may contain black specks from the molding process. The discolored material does not enter the fluid path but may cause therapy delays.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide in the USA.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product was distributed nationwide.
Inventia Healthcare Limited is recalling 13,567 bottles of Chlorthalidone 25 mg tablets because they failed dissolution specifications. The recall is nationwide.
Star Meat Delivery Inc. is recalling raw pork, beef, and goat products produced without federal inspection and bearing false USDA marks.
Nova Bus is recalling 2024-2025 LFS transit buses because an improperly tightened emergency brake valve may cause air leaks and unintentional parking brake activation.
Ford is recalling 2024-2026 Ranger vehicles with 10.1-inch center stack screens that may lose power and fail to display the rearview camera image, increasing crash risk.
Ford is recalling specific 2025-2027 Expedition and F-Series Super Duty vehicles because contaminated LED chips in the headlights may cause a loss of exterior lighting, increasing crash risk.
Ford is recalling 2026 Ranger vehicles because the center screen may lose power, preventing the rearview camera image from displaying and increasing crash risk.
Forest River is recalling 2026-2027 Dynamax Grand Sport GT recreational vehicles because an improperly installed engine pre-heat pump may cause coolant hose failure and engine overheating.
Winnebago is recalling 2027 Arka recreational vehicles because the rear Gross Axle Weight Rating and tire inflation data on the federal placard are incorrect.
Volvo Bus is recalling 2009-2025 9700 buses because the emergency exit label on the entrance door is missing operating instructions, which may delay evacuation.
REV is recalling specific 2025-2027 recreational vehicles because the RoadWatch Safety System may have incorrect programming, potentially disabling safety features.
Colerinsec is recalling Jerify Magnetic Humanoid Toy Sets because loose magnets can be swallowed, posing a risk of serious injury or death to children.