The Recall Desk

State

Florida product recalls

72,820 recalls have nationwide distribution and so reach Florida. 12,816 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,816
Critical
1,763
Severe
2,974
Most recent
2026-09-06

Of the 12,816 recalls naming Florida we have scored against our rubric, 1,763 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,974 (23%) are Severe.

These figures cover only the 12,816 recalls whose distribution notice names Florida specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

126–150 of 85636

  • HighNHTSA·26V555000·2026-08-31

    Jayco Recalls 2027 Entegra Qwest and Melbourne Prestige RVs

    Jayco is recalling certain 2027 Entegra Qwest and Jayco Melbourne Prestige recreational vehicles due to a taillight harness defect that may cause incorrect warning lights on the instrument panel.

    Product
    JAYCO — JAYCO, ENTEGRA MELBOURNE PRESTIGE, QWEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V553000·2026-08-28

    Magic Tilt Watercraft Trailers Recalled Due to Winch Weld Failure

    Magic Tilt is recalling 2025-2026 aluminum watercraft trailers because the winch weld may fail, causing the winch to detach and potentially injure nearby people.

    Product
    MAGIC TILT — MAGIC TILT ALUMINUM WATERCRAFT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V552000·2026-08-28

    Jayco Recalls 2027 Heartland Bighorn Trailers Due to Incorrect Weight Labels

    Jayco is recalling 2027 Heartland Bighorn recreational trailers because the Gross Axle Weight Rating on the certification label may be incorrect, potentially leading to overloading.

    Product
    HEARTLAND — HEARTLAND BIGHORN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26726·2026-08-27

    Walmart Recalls Mainstays Nine-Drawer Fabric Dressers Due to Tip-Over Risk

    Walmart is reannouncing a recall of Mainstays 9-Drawer Fabric Dressers because they pose tip-over and entrapment hazards that can cause serious injury or death to children.

    Product
    Mainstays 9-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26723·2026-08-27

    Steelite Pressure Washers Recalled for Shock and Electrocution Hazards

    Steelite electric pressure washers are recalled because they lack a ground-fault circuit-interrupter and adequate power cord, posing a risk of serious injury or death.

    Product
    Steelite Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V551000·2026-08-27

    Altec Recalls 2021-2023 Service Body Vehicles Due to Fire Risk

    Altec is recalling 2021-2023 Service Body vehicles because water leaks into strobe lights, causing electrical short-circuits that increase fire risk.

    Product
    ALTEC — ALTEC SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26727·2026-08-27

    Chillife Montessori Baby Toy Sets Recalled for Choking Hazard

    CPSC is recalling Chillife 5-in-1 Montessori Baby Toy Sets because the pull string teething toy violates safety standards and poses a choking risk to children.

    Product
    Chillife 5-in-1 Montessori Baby Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26717·2026-08-27

    Conair Recalls Cuisinart Grill Brushes Due to Ingestion Hazard

    Conair is expanding a recall of over 3.6 million Cuisinart grill brushes because metal wire bristles can detach and be swallowed, posing a risk of serious internal injury.

    Product
    Metal Wire Bristle Grill Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26721·2026-08-27

    Kmaier Infant Walkers Recalled for Serious Fall Hazard

    Kmaier recalls infant walkers that violate safety standards by failing to stop at step edges, posing a risk of serious injury or death.

    Product
    Kmaier Infant Walkers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26722·2026-08-27

    Excel Industries Recalls LED Light Kits for Ride-On Mowers Due to Fire Risk

    Excel Industries is recalling about 1,800 accessory LED light kits for Hustler and BigDog ride-on mowers because the light bars can overheat or produce flames.

    Product
    Accessory LED Light Kits used with certain ride-on mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26718·2026-08-27

    MD Wipe Outz Numbing Tattoo Wipes Recalled for Child Poisoning Risk

    Diamond Wipes International is recalling MD Wipe Outz Numbing Tattoo Wipes because the packaging is not child-resistant, posing a risk of serious injury or death from child poisoning.

    Product
    MD Wipe Outz Numbing Tattoo Wipes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26719·2026-08-27

    HABA Rainbow Rattle Toy Recalled Due to Choking and Ingestion Hazards

    HABA USA is recalling Rainbow Rattle Grasping and Teething Toys because a glued knot can untie, exposing small parts that pose choking and ingestion risks to young children.

    Product
    HABA Rainbow Rattle Grasping and Teething Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26724·2026-08-27

    Little Loves & Co. Recalls Youth Clothing with Drawstrings

    Little Loves & Co. is recalling youth clothing sets with drawstrings due to an entrapment hazard that could cause serious injury or death to children.

    Product
    Little Loves & Co. Youth Clothing with Drawstrings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1240-2026·2026-08-26

    Publix Organic Whole Mixed Berries Recalled for E. coli O145:H28 Contamination

    Publix Super Markets is recalling Organic Whole Mixed Berries due to potential E. coli O145:H28 contamination. Consumers should check expiration dates and return affected products.

    Product
    Organic Whole Mixed Berries, Net Wt. 10 oz (284 g) plastic bags, packed in 8 bags per case of 10 oz each. Keep Frozen. UPC 41415-06753
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·H-1241-2026·2026-08-26

    Publix Recalls Organic Whole Mixed Berries Due to E. coli Contamination

    Publix Super Markets is recalling Organic Whole Mixed Berries due to potential E. coli O145:H28 contamination. The product was distributed in eight southeastern states.

    Product
    Organic Whole Mixed Berries, Net Wt. 48 oz (3Lb) plastic bag. packed in 6 bags per case of 10 oz each. Keep Frozen. UPC 41415-12153
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·H-1242-2026·2026-08-26

    Coast Tropical Jalapeno Peppers Recalled for Potential Salmonella Javiana Contamination

    Coast Citrus Distributors is recalling bulk jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed to wholesale distributors and has not been sold at retail.

    Product
    Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging. Packaged in assorted bulk package sizes (10lbs, 40lbs, 35lbs, 20lbs, 38lbs 1 1/9 Bushel) ; Product of MX; Coast Tropical TX UPCs 73296608113; 73296600558; 73296610927; 73296600559; 732966107055; 02060042
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1239-2026·2026-08-26

    Publix Recalls Organic Whole Blueberries Due to E. coli Contamination Risk

    Publix Super Markets is recalling 37,260 units of Organic Whole Blueberries due to potential E. coli O145:H28 contamination. The product was distributed in eight southeastern states.

    Product
    Organic Whole Blueberries, Net Wt. 48 oz (3Lb) plastic bag, packed in 6 bags per case of 10 oz each. Keep Frozen. UPC 41415-12053
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Drugs)·D-0788-2026·2026-08-26

    Fresenius Kabi Recalls Morphine Syringes Due to Labeling Error

    Fresenius Kabi is recalling 625,500 Morphine Sulfate syringes because some were mislabeled and contained Dilaudid instead.

    Product
    MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1238-2026·2026-08-26

    Publix Organic Whole Blueberries Recalled for E. coli O145:H28 Contamination

    Publix Super Markets is recalling Organic Whole Blueberries due to potential E. coli O145:H28 contamination. Consumers should check expiration dates and discard affected products.

    Product
    Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each. Keep Frozen UPC 41415-06453
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0793-2026·2026-08-26

    American Regent Recalls Cyanocobalamin Injections Due to Particulate Matter

    American Regent, Inc. is recalling specific lots of Cyanocobalamin injections due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    CYANOCOBALAMIN — CYANOCOBALAMIN (CYANOCOBALAMIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0797-2026·2026-08-26

    American Regent Recalls Acetylcysteine Solution Due to Particulate Matter

    American Regent, Inc. is recalling Acetylcysteine Solution USP due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    ACETYLCYSTEINE — ACETYLCYSTEINE (ACETYLCYSTEINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2976-2026·2026-08-26

    Siemens Recalls Emit 2000 Quinidine Assay Due to Precision Issues

    Siemens Healthcare Diagnostics is recalling specific lots of the Emit 2000 Quinidine Assay because unacceptable precision may cause falsely high results, risking improper patient treatment.

    Product
    Beckman Coulter, Emit 2000 Quinidine Assay REF: OSR4Q229 Contents: R1: 2 x 23 mL;R2 2x13 mL
    Category
    Medical Device
    Distribution
    Distributed nationwide