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.
CASE v7.0 Cardiac Testing Systems are being recalled because electrical sparking may occur at the printer head, and ignition of thermal paper could cause serious thermal injury.
Albertsons store-made Peanut Butter Chocolate Chip Bar with Pretzel is being recalled because the contains statement does not declare almond. 128 units are affected.
Albertsons store-made ahi poke products, sold under three UPCs, are being recalled because the contains statement does not declare tuna. 23 units in total are affected.
Albertsons store-made Platter Cheeses of France is being recalled because the contains statement does not declare almond. 31 units are affected.
The Large Volume Pump of the Ivenix Infusion System is being recalled because of the potential for the Cassette Loading Lever to break. 18,444 installed bases are affected.
PhaseOne Antimicrobial Solution is being recalled because the stainless steel spring inside the sprayer can corrode, releasing trace metallic elements into the solution.
Good Neighbor Pharmacy Extra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Albertsons store-made Artisan White Strawberry Cake Bar is being recalled because the contains statement does not declare almond. 173 units are affected.
Equaline Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
TopCare Health Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
BD Pyxis MedStation ES Tower medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Tums Antacid Assorted Fruit tablets, calcium carbonate 1000 mg in 160-count bottles, are being recalled because of small metallic particles in the chewable tablets.
TopCare Health Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
The BD Pyxis MedStation 4000 medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Albertsons store-made Ready Meals Salad Waldorf is being recalled because the contains statement does not declare walnut. 82 units are affected.
Albertsons store-made Boston Creme Dubai 5-inch cake is being recalled because the contains statement does not declare pistachio. 25 units are affected.
Albertsons store-made 8-inch two-layer carrot cakes are being recalled because the contains statement does not declare pecan or walnut. 167 units are affected.
Albertsons store-made Cheesecake Slice Colossal Dubai is being recalled because the contains statement does not declare pistachio. 32 units are affected.
Denago EV is recalling 2024-2026 electric vehicles that may fail to emit pedestrian warning sounds, increasing the risk of crashes.
Albertsons store-made Lox Avocado Toast is being recalled because the contains statement does not declare salmon. 19 units are affected.
Lannett Niacin Extended-release Tablets, 1,000 mg, are being recalled after a stability test returned an out-of-specification low result for Stage 3 dissolution at 24 hours.
Arvis Hip & Knee 3.0 Instrument Sets are being recalled because the V-Block Assembly and Trackers A, B, C and E may show early wear or corrosion on the exposed magnet face.
The BD Pyxis Anesthesia Station ES is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 4,579 units affected.
Equaline Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Lidocaine HCl Injection USP in 5 mL single-dose ampules distributed by Spectra Medical Devices is being recalled for lack of assurance of sterility. 210,625 ampules affected.