State
73,218 recalls have nationwide distribution and so reach Florida. 12,856 additional recalls listed Florida specifically in their distribution scope.
Of the 12,856 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 2,991 (23%) are Severe.
Which agencies issued them
These figures cover only the 12,856 recalls whose distribution notice names Florida specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Paradise Flavors LLC is recalling Blackberry Cheesecake ice cream (4 oz) due to undeclared milk, soy, and wheat allergens. The product was distributed in Florida.
Paradise Flavors frozen key lime pie contains undeclared allergens (milk, soy, wheat) and color additives (FD&C yellow #5, blue #1, red #40). Consumers with allergies should not consume this product.
Paradise Flavors LLC is recalling peanut butter ice-cream base distributed in Florida due to undeclared allergens (milk, peanut, soy, and wheat) not listed on the label.
Paradise Flavors LLC is recalling vanilla ice cream base due to undeclared milk allergen and color additives. Consumers with milk allergies should not use this product.
Paradise Flavors LLC is recalling Chocolate with Almonds ice-cream products due to undeclared allergens: milk, tree nuts, peanuts, and soy. Consumers with these allergies should discard the product.
Paradise Flavors recalls Sweet Corn ice cream mix distributed in Florida for undeclared milk allergen and color additives. Consumers with milk allergies risk allergic reaction from this product.
A software bug in Philips Brilliance CT scanners causes image-fusion errors, resulting in incorrect radiation therapy coordinates and potential treatment planning failures.
Volvo Trucks is recalling certain 2023-2024 VN trucks because the accelerator pedal position sensor may disconnect, preventing the engine from returning to idle quickly. This can cause loss of vehicle control and increase crash risk.
Microbiologics Inc recalls KWIKSTIK microbiological reagent kits due to Aspergillus flavus contamination in bulk pellets. Affected products were distributed worldwide, including the US, Italy, France, Turkey, Peru, and Mexico.
The IBA Proton Therapy System's patient positioning system can perform unexpected motions, risking patient crushing. Five US units and nine international units are affected.
Medline is recalling 4,850 adult blood culture collection kits (lot numbers 23EMI373, 23EMF712, 23DMF155, 23CMH026) because components inside expired before the kit's labeled expiration date.
Physio-Control is recalling LIFEPAK 15 defibrillators due to a potential defect where battery pins may become loose, causing power issues.
Physio-Control is recalling LIFEPAK 15 defibrillators due to loose battery pins that may cause power failure. Users should verify device functionality immediately.
Physio-Control is recalling LIFEPAK 15 defibrillators due to potential loose battery pins that could cause power failure. Four affected units have been distributed to Arizona, California, North Carolina, New Jersey, and New York.
Physio-Control has recalled LIFEPAK 15 defibrillators because battery pins may become loose, causing power issues. Owners should contact the manufacturer for instructions on how to proceed.
Ricon is recalling Threshold Warning System Kits for wheelchair lifts because the red beacon may not be bright enough, increasing injury risk.
Atrium Medical Corporation is recalling Express Dry Seal Chest Drains (models 4000-100N and 4050-100N) due to inadequate instructions for proper catheter and patient tube connection setup. No injuries have been reported.
Philips Spectral CT on Rails software version 5.1.0 may fail to move the needle position to the desired location during scans. This could cause the gantry to move unexpectedly and potentially collide with the user or needle.
Microbiologics Inc is recalling LYFO-DISK P. venetum laboratory culture disks (lot 794-142) found contaminated with Aspergillus flavus during complaint investigation. The product was distributed worldwide.
Physio-Control is recalling 8 LIFEPAK 15 defibrillators due to loose battery pins that may cause power loss. Affected units were distributed in Arizona, California, North Carolina, New Jersey, and New York.
Mack is recalling 650 2023–2024 trucks due to a sensor defect that can prevent the engine from returning to idle quickly, risking loss of vehicle control. The company will replace the throttle pedal and update software at no cost.
Medline's blood culture kit is being recalled because components inside the kit have expired before the kit's stated expiration date. This could affect the kit's ability to function properly.
Medline Industries is recalling 3,160 units of 24 Blood Culture Kits because components within the kit have expired before the overall kit's stated expiration date. Expired components may compromise device performance or test result accuracy.
Certain 2024 Land Rover Range Rovers may have improperly secured engine oil cooler hoses that could leak oil onto roadways, creating a hazard for other drivers and increasing crash risk.
General Motors recalls certain 2024 Chevrolet Silverado EV vehicles due to improperly tightened front seat belt buckle attachment bolts that may not restrain occupants properly during a crash.