The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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26–50 of 89362

  • HighCPSC·26740·2026-09-03

    Truststone Recalls XO Poppy Magnetic Wireless Power Banks Due to Fire Hazards

    Truststone Group is recalling XO Poppy Power Trip Magnetic Wireless Power Banks because the lithium-ion batteries can overheat and ignite, posing fire and burn risks.

    Product
    XO Poppy Power Trip Magnetic Wireless Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26741·2026-09-03

    Clorox Recalls Scented Mistolin and Lestoil Cleaners in Puerto Rico

    Clorox is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands due to potential bacterial contamination.

    Product
    Scented Mistolin® Dilutable Cleaners and Lestoil® Heavy Duty Multi-Purpose Cleaners sold in Puerto Rico and the U.S. Virgin Islands.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1259-2026·2026-09-02

    FDA Recalls Glutinous Rice Balls with Undeclared Peanuts

    KHONG GUAN (HQ) is recalling Glutinous Rice Balls with Black Sesame Filling due to undeclared peanuts. The product was distributed in eight US states.

    Product
    Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·H-1262-2026·2026-09-02

    Sirna & Sons Jalapeno Peppers Recalled for Potential Salmonella Javiana

    Sirna & Sons Produce is recalling 249 bags of 1 lb jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed for food service use in Ohio and Pennsylvania.

    Product
    Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB, repackaged into 1 lb. plastic bags, Product Number: 55255, Packed by Sirna & Sons Produce 7176 State Route 88, Ravenna, OH 44266, distributed for food service use only
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·H-1301-2026·2026-09-02

    Jaime's Foods ATX Recalls Jalapeno Ranch Due to Undeclared Egg Allergen

    Jaime's Foods ATX, LLC is recalling Jalapeno Ranch in 16 oz. glass jars because the product contains an undeclared egg allergen. The recall affects 102 cases distributed in Texas.

    Product
    Jalapeno Ranch, packed in 16 oz. glass jars, 6 jars per case, with UPC #199284564923.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-1263-2026·2026-09-02

    FDA Recalls Addall XR Shot Liquid Dietary Supplement

    ZMB Enterprises is recalling Addall XR Shot liquid dietary supplements because they contain undeclared ingredients 1,4-DMAA, Phenylethylamine, and Phenibut.

    Product
    Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-1266-2026·2026-09-02

    Outshine Fruit Bars Grape Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars Grape due to the potential presence of glass pieces.

    Product
    Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2991-2026·2026-09-02

    Medline Neonatal Heated Wire Breathing Circuits Recalled for Thermal Failure

    Medline is recalling 20 units of neonatal heated wire breathing circuits due to potential thermal damage that could cause airway obstruction or respiratory distress in infants.

    Product
    Medline Hudson RCI, DBD-CIRCUIT,VENT,INSPIRATORY,HEATED,NEO, Medline Product Number/SKU HUD78019 (Teleflex Product Number/SKU 780-19); breathing circuit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1268-2026·2026-09-02

    Outshine Black Cherry Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Black Cherry Fruit Bars because they may contain glass pieces. Consumers should stop eating the product.

    Product
    Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UPC 041548000121, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0776-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 50 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1265-2026·2026-09-02

    Outshine Watermelon Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Watermelon Fruit Bars because they may contain glass pieces.

    Product
    Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2993-2026·2026-09-02

    Medline Neonatal Heated Wire Breathing Circuits Recalled for Thermal Damage Risk

    Medline is recalling neonatal and infant heated wire breathing circuits due to a risk of sporadic failure and thermal damage at the humidifier connector.

    Product
    Medline breathing circuits labeled as: 1) MEDLINE HUDSON RCI, CIRCUIT, NEO, SING LIMB, HTD,COLUMN, Medline Product Number/SKU HUD78001KIT (Teleflex Product Number/SKU 780-01KIT); 2) MEDLINE HUDSON RCI, CIRCUIT, NEO, DUAL LIMB HTD, COLUMN, Medline Product Number/SKU HUD78007K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0785-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 200 mcg tablets because they are subpotent. The recall covers distribution nationwide in the United States.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0778-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·N/A·2026-09-02

    White Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient

    Shaman Botanicals, LLC is recalling White Vein Advanced Alkaloids Chewable Tablets because testing found the active ingredient 7-hydroxymitragynine is present in a quantity greater than the labeled specification.

    Product
    Clear glass bottle with black screw lid with multi label which reads in part as "***AFRICANDO FOODS, LLC ALFREDO HOT SAUCE, Net Weight 8 oz. ***INGREDIENTS: Habenaro Peppers, Garlic, Onions, Water, Distilled 5% White Vinegar, Spices***Manufactured and Packed By Africando Foods, L
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·H-1267-2026·2026-09-02

    Outshine Tangerine Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Tangerine Fruit Bars because they may contain glass pieces.

    Product
    Outshine Fruit Bars Tangerine, 6-Count 2.5 ounce, with UPC 041548612041, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0779-2026·2026-09-02

    Accord Healthcare Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 100 mcg tablets because they may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0832-2026·2026-09-02

    B. Braun Recalls Lactated Ringer's Injection Due to Particulate Matter

    B. Braun Medical Inc. is recalling 23,688 bags of Lactated Ringer's Injection USP due to the presence of particulate matter.

    Product
    LACTATED RINGERS — LACTATED RINGERS (SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1264-2026·2026-09-02

    Outshine Strawberry Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Strawberry Fruit Bars because they may contain glass pieces.

    Product
    Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·H-1269-2026·2026-09-02

    Outshine Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars because they may contain glass pieces. Consumers should check for specific batch codes.

    Product
    Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine. 24-Count 2.5 ounce, UPC 041548816678, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·H-1260-2026·2026-09-02

    KHONG GUAN Recalls Rice Balls Due to Undeclared Peanuts

    KHONG GUAN is recalling Black and White Glutinous Rice Balls with Black Sesame Filling because they contain undeclared peanuts.

    Product
    BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000084
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0803-2026·2026-09-02

    ACTHAR Gel Recalled for Presence of Glass and Stopper Particulate Matter

    Mallinckrodt is recalling ACTHAR Gel vials due to the presence of glass and stopper pieces. Patients should stop using the product and contact their healthcare provider.

    Product
    ACTHAR — ACTHAR (REPOSITORY CORTICOTROPIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0786-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling Levothyroxine Sodium 300 mcg tablets because they may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0827-2026·2026-09-02

    Fresenius Kabi Recalls Tyenne Injection Due to Glass Particles

    Fresenius Kabi is recalling Tyenne (tocilizumab-aazg) injection vials because an internal investigation found the presence of glass particles.

    Product
    TYENNE — TYENNE (TOCILIZUMAB-AAZG)
    Category
    Drug
    Distribution
    Distributed nationwide