The Recall Desk

State

Florida product recalls

73,218 recalls have nationwide distribution and so reach Florida. 12,856 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,856
Critical
1,775
Severe
2,991
Most recent
2026-10-06

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.

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.

15251–15275 of 86074

  • ModerateFDA (Drugs)·D-0112-2024·2023-11-29

    Prescription esomeprazole magnesium capsules recalled for failed impurity specifications

    Glenmark Pharmaceuticals recalled esomeprazole magnesium 20mg capsules nationwide due to out-of-specification organic impurities detected during stability testing. No illnesses have been reported.

    Product
    ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0379-2024·2023-11-29

    Compress Device Short Anchor Plug recalled for potential metal burrs

    Biomet recalls Compress Device Short Anchor Plug devices due to potential metal burrs in transverse holes that may prevent proper drill and pin placement during orthopedic surgery, affecting units distributed worldwide.

    Product
    Compress Device Short Anchor Plug, 12 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178554
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0370-2024·2023-11-29

    Orthopedic Anchor Plugs Recalled for Metal Burrs Preventing Proper Installation

    Biomet is recalling Compress Device Segmental Anchor Plugs due to metal burrs in transverse holes that may prevent drills or pins from passing through, potentially extending surgical procedures.

    Product
    Compress Device Segmental Anchor Plug, 10 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0114-2024·2023-11-29

    Lisinopril Tablets Recalled for Stray Amlodipine Tablet Contamination

    NCS Healthcare recalled Lisinopril Tablets USP 20 mg nationwide due to potential presence of stray Amlodipine Besylate 10 mg tablets in certain lots. No illnesses have been reported.

    Product
    BUSPIRONE HYDROCHLORIDE — BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0380-2024·2023-11-29

    Compress Device Short Anchor Plugs recalled due to metal burrs

    Biomet is recalling Compress Device Short Anchor Plugs (14 MM) due to potential metal burrs in transverse holes that may prevent proper insertion during surgery. The defect may extend surgical time.

    Product
    Compress Device Short Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178556
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V803000·2023-11-28

    Cake Recalls 2020-2022 Osa Flex Electric Mopeds for Steering Defect

    Cake is recalling 2020-2022 Osa Flex electric mopeds because the aluminum steering column may fatigue and break, causing a sudden loss of steering.

    Product
    CAKE — CAKE OSA FLEX ELECTRIC MOPED
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V800000·2023-11-28

    2024 Ford Mustang brake pedal defect increases crash risk

    Ford is recalling certain 2024 Mustang vehicles because the brake pedal assembly may have been manufactured incorrectly, causing a loose brake pedal. A loose brake pedal can result in loss of braking function, increasing the risk of a crash.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E092000·2023-11-28

    Chrysler Recalls Steering Column Control Modules for Signal Confusion

    Chrysler is recalling 1,240 Mopar steering column control modules that may cause high beams and turn signals to activate incorrectly, increasing crash risk.

    Product
    STEERING:STEERING CONTROL MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V799000·2023-11-28

    RAM 2500 Steering Control Module Failure May Disable Turn Signals and High Beams

    Certain 2023-2024 RAM 2500 vehicles and related models have a faulty steering column control module that may cause turn signals and high beams to malfunction, increasing the risk of a crash. Owners should contact FCA US, LLC for free repairs.

    Product
    RAM — RAM 4500, 5500, 3500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V798000·2023-11-26

    KME Fire Trucks Recalled for Parking Brake Defect

    KME is recalling 2021-2023 fire trucks because a valve defect may delay parking brake engagement, increasing crash risk.

    Product
    KME — KME redundant PREDATOR, SEVERE SERVICE, PREDATOR, redundant PANTHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V797000·2023-11-24

    BMW Recalls 2014-2015 X3, X4, and X5 Models for Airbag Defect

    BMW is recalling specific 2014-2015 X3, X4, and X5 vehicles because the driver's airbag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    BMW — BMW X4, X3, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V795000·2023-11-23

    Micro Bird Recalls G5 School Buses Due to Wheelchair Track Defect

    Micro Bird is recalling certain G5 school buses because wheelchair track anchorages may detach during a crash, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0443-2024·2023-11-22

    Frozen Ice Cream Base Recalled for Undeclared Milk Allergen and Food Colorings

    Paradise Flavors LLC recalls Dulce de Leche ice-cream base (4 oz) for undeclared milk allergen and color additives. The recall affects 210 units distributed in Florida.

    Product
    DULCE DE LECHE, Ice-cream base, Natural flavor, artificial flavor and coloring., Distributed By Paradiose Flavors LLC. 4oz (120 mL). Packaged in plastic pouch. Frozen.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0429-2024·2023-11-22

    Paradise Flavors frozen cappuccino ice-cream recalled for undeclared milk

    Paradise Flavors LLC is recalling 60 units of its frozen cappuccino ice-cream (4 oz pouches) from Florida due to undeclared milk allergen, which poses a serious risk to consumers with milk allergies.

    Product
    CAPPUCCINO, Ice-cream base, natural flavoring, artificial flavoring. PARADISE FLAVORS. 4 oz. Packaged in plastic pouch. Frozen.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0440-2024·2023-11-22

    Paradise Flavors frozen mamey recalled for undeclared milk allergen

    Paradise Flavors LLC is recalling 80 units of frozen MAMEY product due to undeclared milk allergen. Consumers with milk allergies should not consume this product.

    Product
    MAMEY, PARADISE FLAVORS LLC, 4 oz. Packaged in plastic pouch. Frozen.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0455-2024·2023-11-22

    Coconut ice cream mix recalled for undeclared milk and tree nut allergens

    Paradise Flavors LLC is recalling 216 units of COCONUT/COCO ice cream mix from Florida distribution due to undeclared milk and tree nut allergens. Consumers allergic to milk or tree nuts should not consume this product.

    Product
    COCONUT/COCO ice cream mix, natural flavors, artificial flavors. 9601 Overseas Hwy, Marathon FL. 100ml 3 oz. Packaged in plastic pouch. Frozen.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0449-2024·2023-11-22

    Cookies And Cream Frozen Product Recalled for Undeclared Milk, Soy, and Wheat Allergens

    Paradise Flavors LLC is recalling 318 units of Cookies And Cream frozen product (4 oz) due to undeclared allergens: milk, soy, and wheat. The product was distributed in Florida.

    Product
    Cookies And Cream, distributed by Paradise Flavors LLC, 4 OZ, 120ML, Packaged in plastic pouch. Frozen.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0424-2024·2023-11-22

    Mint Chocolate Chip Ice Cream Recalled for Undeclared Milk and Color Additives

    Paradise Flavors LLC is recalling 112 units of Mint Chocolate Chip ice cream for containing undeclared milk and food color additives (FD&C yellow #5, blue #1, red #40). The product was distributed in Florida.

    Product
    MINT CHOCOLATE CHIP, Ice-cream base, Chocolate chips, Artificial Flavoring, Artificial color. PARADISE FLAVORS. 4 oz. Packaged in plastic pouch. Frozen.
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·23V789000·2023-11-22

    Land Rover Defender Recall for Brake Caliper Detachment Risk

    Jaguar Land Rover is recalling 121 modified 2023 Defender 130 vehicles because improperly reinstalled brake calipers may detach, reducing braking ability and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0433-2024·2023-11-22

    Ice Cream Base Recalled for Undeclared Milk Allergen and Food Dyes

    Paradise Flavors LLC is recalling RUM RAISIN ice-cream base (4 oz frozen pouches) distributed in Florida due to undeclared milk allergen and undeclared food dyes (FD&C yellow #5, red #40, blue #1). Consumers with milk allergies should not consume this product.

    Product
    RUM RAISIN, ice-cream base, artificial flavoring natural fruits, artificial. DISTRIBUTED PARADISE FLAVORS LLC. 4 oz. Packaged in plastic pouch. Frozen.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0428-2024·2023-11-22

    Pink Guaba Ice Cream Mix Recalled for Undeclared Milk Allergen and Color Additives

    Paradise Flavors LLC recalls Pink Guaba ice cream mix due to undeclared milk allergen and color additives. Consumers with milk allergies should not consume this product.

    Product
    PINK GUABA, Ice-cream mix, filtered water, Natural Flavoring, sugar, Artificial color. PARADISE FLAVORS. 4 oz. Packaged in plastic pouch. Frozen.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0452-2024·2023-11-22

    EZQUIMAL Ice Cream Base Recalled for Undeclared Allergens and Color Additives

    Paradise Flavors LLC recalls EZQUIMAL 4 oz frozen ice-cream base due to undeclared allergens (milk, tree nuts, peanuts, soy) and color additives. Product distributed in Florida.

    Product
    EZQUIMAL, ice-cream base, natural flavoring, chocolate cover, penuts. 4 OZ. DISTRIBUTED BY PARADISE FLAVORS LLC. Packaged in plastic pouch. Frozen.
    Category
    Food
    Distribution
    1 state