State
72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Moonlight Packing is recalling a further 2,622 cases of loose bulk peppermint peaches over potential Listeria monocytogenes contamination, under enforcement record H-0324-2026.
Hudson River Foods is recalling 113 units of Doughy brand Chocolate Chip Cookie Dough because the product may be contaminated with Salmonella. The FDA has classified the action as Class I.
Moonlight Packing is recalling 104 cases of 2 lb bagged white peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen jamun after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Stuffed Foods is recalling 51 cases of Cacio e Pepe Arancini over undeclared soy protein concentrate. The FDA has classified the action as Class I.
ByHeart is recalling 3,482,131 cans and 3,531,901 single serve packets of Whole Nutrition Infant Formula after contamination with Clostridium botulinum. The FDA has classified the action as Class I.
Moonlight Packing is recalling 2,603 cases of loose bulk peppermint peaches over potential contamination with Listeria monocytogenes, under enforcement record H-0323-2026.
Moonlight Packing is recalling 439 bags of 4-count Peppermint Peach packs over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Suzuki is recalling 2025-2026 DR-Z400S and 2025 DR-Z400SM motorcycles because incorrectly tightened screws may allow brake fluid to leak, reducing braking ability.
Rollx Vans is recalling certain converted vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints, because the retractors may not lock and the wheelchair may not be properly secured.
BMW is recalling specific 2014-2015 2, 3, and 4 Series vehicles because the head air bag inflator may fail, posing an injury risk during a crash.
Autocar is recalling one 2024 E-ACTT terminal tractor because improperly secured battery cable connections may overheat and cause a fire or loss of motive power.
Toyota is recalling certain 2024-2025 Highlander and Highlander Hybrid vehicles because the third row centre seat belt roof anchor may have been installed at an incorrect angle.
Vantage Mobility is recalling 2021–2025 Chrysler Pacifica vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints because the retractors may fail to lock, allowing wheelchairs to move unsecured during transit.
Medline is recalling 15 Medline Perfusion Syringes because they contain BD Luer Tip Caps from trays that failed routine biocompatibility testing.
Cipla USA is recalling 63,504 bottles of Cinacalcet Hydrochloride Tablets, 30 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.
Kia is recalling certain 2023-2025 Sportage and Sportage Plug-In Hybrid vehicles with a 4.2-inch screen and a Kia tow hitch harness, because a software error may make the instrument panel screen fail.
Bard Peripheral Vascular is recalling 1,240 Safe-T-Centesis 6 Fr Catheter Drainage Trays because the safety indicator can show the catheter in the sharp position when it is blunt.
Gimme Coffee is recalling 252 boxes of gimme! Decaf de Agua coffee pods because the outer packaging is labelled decaf while the pods inside are caffeinated Deep Disco pods.
Cipla USA is recalling 12,576 bottles of Cinacalcet Hydrochloride Tablets, 90 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.
Bell Sports is recalling Scout Air helmets in sizes S and L because they may lack proper penetration protection, failing federal safety standards.
Orthofix U.S. is recalling 40,956 CONSTRUX Mini Ti Spacer System units because the labeling contains claims that are not consistently present.
Nipro Medical is recalling Surdial DX Hemodialysis Systems because a screw may loosen or fall out of the system.
Winder Laboratories is recalling 3,528 bottles of Morphine Sulfate Oral Solution because the size stated on the carton label did not match the size of the bottle inside.
Steris is recalling 10 AMSCO 7052HP Washer/Disinfectors because a wire connected to the electrical box may shift out of position, which may result in electrical arcing inside the unit.