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 the agency’s own highest classification or reported deaths or serious injuries, 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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13251–13275 of 114070

  • HighFDA (Food)·F-0001-2025·2024-10-09

    KARA BOONDHI Recalled for Undeclared Wheat Allergen

    Grace Imports is recalling KARA BOONDHI due to undeclared wheat allergen on the label. The affected product was distributed to retail stores in Georgia.

    Product
    KARA BOONDHI INGREDIENTS: Gram flour, Edible beg oil (Refined Palmolein Oil), Chilly powder, Curry leaf, pepper, Asafoetida, Corn Flour, Urid dhall, Black salt. Natural Antioxidant (Mixed Tocopherol INS 305) ALLERGEN INFORMATION: Made in a FActory that Process Peanuts, Tree…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0006-2025·2024-10-09

    Sqwincher Electrolyte Beverage Mix recalled for potential metal contamination

    Kent Precision Foods Group is recalling Sqwincher Electrolyte Beverage Mix (Orange powder, lot 2B0165712) due to potential metal contamination. The product was distributed in 11 states.

    Product
    Sqwincher Electrolyte Beverage Mix, Orange powder pack, Net Wt 47.66 oz (3lb) 1.35 kg: UPC 7588008834 / 16 per case / 5 gal yield item number 159016404
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0019-2025·2024-10-09

    Hemodialysis console blood leak sensor may fail to trigger alarm

    A component in certain Tablo Hemodialysis consoles may fail to detect small blood leaks promptly, potentially causing symptoms like hypotension, fatigue, and dizziness if undetected blood loss occurs.

    Product
    Tablo Console, REF: PN-0003000, PN-0006000, part of the Tablo Hemodialysis System. The Tablo Hemodialysis System is indicated for use in patients with acute and/or chronic renal failure, with or without ultrafiltration, in an acute or chronic care facility.
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-3308-2024·2024-10-09

    DVOT Rapid Antigen Test Kits Recalled for Lack of FDA Authorization

    DVOT antigen test kits lack FDA authorization for US sale. Approximately 50,000 unauthorized kits were distributed. Users should discontinue use immediately due to unvalidated safety and accuracy.

    Product
    DVOT SARS-CoV-2 & RSV &MP &ADV & FIu A/B Antigen Combo Test Kit, Model Number ACT01
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0007-2025·2024-10-09

    Pluvicto Radiopharmaceutical Drug Recalled Due to Manufacturing Quality Deviations

    Advanced Accelerator Applications is recalling 99 doses of Pluvicto (lutetium LU-177 injection) due to manufacturing quality deviations. The affected lots were distributed to six states.

    Product
    Pluvicto, 1000 MBq/mL (27 mCi/mL), lutetium, LU 177, vipivotide tetraxetan injection, Single-dose vial, Sterile, Manufacturer Advanced Accelerator Applications, 57 E. Willow Street, NJ 07041, Millburn USA. NDC 69488-0010-61
    Category
    Drug
    Distribution
    6 states
  • HighFDA (Devices)·Z-3312-2024·2024-10-09

    Medical Display Unit Recalled for Unintended Touch Input During Patient Monitoring

    Philips DIVA 24-inch touch display may generate unintended touch inputs, risking erroneous acknowledgement of patient alarms and delayed detection of patient condition changes. No injuries have been reported.

    Product
    DIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX system central monitoring system. Model: RGD2461AMI Philips Part # 866126
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0004-2025·2024-10-09

    Ceremonial Cacao Paste Recalled for Elevated Lead Levels

    Heart of the Earth ceremonial cacao paste is being recalled due to elevated lead levels in the product. Consumers should not consume this product and should contact a healthcare provider if they have concerns.

    Product
    Heart of the Earth (HOTE) 100% Pure Ceremonial Cacao Pre-Ground Paste. Net Wt. 16oz (454g). Packaged in Kraft paper heat sealed stand-up pouch bags with inner plastic liner with SKU PC-GRUCCP-1LB. Product of Guatemala. Distributed Soul Lift Cacao of Portland, Oregon. The…
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0003-2025·2024-10-09

    Spicy Murukku Snack Recalled for Undeclared Wheat Allergen

    Grace Imports is recalling Spicy Murukku snack due to undeclared wheat on the label. Consumers with wheat allergies face serious health risks from unlabeled exposure.

    Product
    SPICY MURUKKU INGREDIENTS: Rice Flour, Edible Veg Oil (Refined Palmolein Oil), Salt, Salt, Chilly powder, Roasted Bengal Gram Flour***Asafoetida, Natural Antioxidant (Mixed Tocopherol INS 305) ALLERGEN INFORMATION: Made in a Factory that Process Peanuts, Tree nuts, Soy, Milk…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0017-2025·2024-10-09

    Chocolate chip muffins recalled for undeclared milk and wheat

    The Posh Bakery is recalling Whole Grains chocolate chip muffins due to undeclared milk and wheat allergens with missing allergen labeling. Those with milk or wheat allergies should not consume this product.

    Product
    Whole Grains Bakery labeled "Choclate Chip Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC"7 13583 05 105 4"
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0021-2025·2024-10-09

    Carrot Muffins Recalled for Undeclared Milk, Wheat, and Coconut Allergens

    The Posh Bakery is recalling Carrot Muffins due to undeclared whey (milk), wheat flour, and coconut allergens, plus missing nutrition facts and allergen labeling. Consumers with allergies should not consume this product.

    Product
    Whole Grains Bakery labeled "Carrot Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC"7 13583 05 108 5"
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0012-2025·2024-10-09

    Big Bottom Milk Company Chocolate Milk Recalled for Inadequate Pasteurization

    Big Bottom Milk Company is recalling chocolate milk that was not properly pasteurized. The recall affects 251 units distributed to Georgia, North Carolina, and South Carolina.

    Product
    BIG BOTTOM MILK COMPANY, CHOCOLATE MILK GRADE A, 1 US Half Gallon (1.89 liters), Big Bottom Milk Company 221 Hogan Rd, Forest City, NC, Expiration Date 09/09/2024 UPC code 850061506054
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0014-2025·2024-10-09

    Poppy Seed Muffins Recalled Due to Undeclared Milk, Wheat, and Almond Allergens

    The Posh Bakery is recalling 6-ounce Poppy Seed Muffins due to undeclared milk (whey), wheat, and almond allergens. The product lacks required allergen labeling, posing a risk to consumers with allergies.

    Product
    Whole Grains Bakery labeled "Poppy Seed Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC "7 13583 05 103 0"
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0007-2025·2024-10-09

    Sqwincher Electrolyte Beverage Mix Recalled for Potential Metal Contamination

    Kent Precision Foods Group is recalling Sqwincher Electrolyte Beverage Mix in four flavors due to potential metal contamination. The affected powdered beverages were distributed across 11 states.

    Product
    1. Sqwincher Electrolyte Beverage Mix, orange powder packs, Net Wt 23.83 oz (1 lb 8 oz) 675.6 g: UPC 7588025004; packaged in assorted case, 32 per case / 2.5 gal yield item number 159016044 2. Sqwincher Electrolyte Beverage Mix, grape powder packs, Net Wt 23.83 oz (1 lb 8 oz)…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0020-2025·2024-10-09

    Banana nut muffins recalled for undeclared milk and wheat allergens

    The Posh Bakery recalls Whole Grains Bakery Banana Nut Muffins (6 oz) due to undeclared milk and wheat allergens. The muffins lack required allergen-contains statements and nutritional fact labels.

    Product
    Whole Grains Bakery labeled "Banana Nut Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC"7 13583 05 101 6"
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0013-2025·2024-10-09

    Big Bottom Milk Chocolate Milk Recalled for Inadequate Pasteurization

    Big Bottom Milk Company is recalling 701 units of Chocolate Milk Grade A (1-pint bottles) distributed in Georgia, North Carolina, and South Carolina due to failure to achieve required pasteurization temperatures.

    Product
    BIG BOTTOM MILK COMPANY, CHOCOLATE MILK GRADE A, 1 US Pint (0.473 liters), Big Bottom Milk Company 221 Hogan Rd, Forest City, NC, Expiration Date 09/09/2024 UPC code 850061506078
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0008-2025·2024-10-09

    Dental Ultrasonic Cleaner Recalled for Bacterial Contamination

    Young Dental Manufacturing is recalling BIOTROL PURIT Clean-It Ultrasonic Cleaner (REF PC016) due to bacterial contamination in the bulk product used for repackaging. The recall affects 1,391 units distributed across 10 states.

    Product
    BIOTROL PURIT Clean-It General Purpose Ultrasonic Cleaner, REF PC016, net contents 16 fl. oz., makes 16 gallons of solution.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Food)·F-1836-2024·2024-10-09

    Mini Raspberry Lemon Coffee Cake Recalled for Undeclared Walnuts and Wheat

    Mini Raspberry Lemon Coffee Cake products in Washington were mislabeled and contain undeclared walnuts and wheat. Consumers with allergies to these ingredients should not consume the product and should return it to the store.

    Product
    Mini Raspberry Lemon Coffee Cake, net wt. 13.5oz. UPC 8 57297 00745 4. Made with Gluten-Free Ingredients in a Gluten-Friendly Bakery. Macrina Bakery - Kent, WA. Ingredients: CANE SUGAR, GREEK YOGURT (GRADE A PASTEURIZED CULTURED MILK, CREAM, NONFAT MILK), EGGS, RASPBERRIES…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0005-2025·2024-10-09

    Sriracha Sauce Recalled for Manufacturing Without Proper Authorization

    Blue Tape Sriracha sauce (136 bottles, 10.5 oz each) was manufactured without the required authorization for producing acidified foods, creating potential safety risks.

    Product
    Blue Tape Sriracha sauce is refrigerated condiment, packaged in a 10.5oz clear squeeze bottle, sold individually. Ingredients: Chilies, Garlic, Capsicum, Sugar, Salt, White Wine Vinegar. There is no company address on the label and no UPC code.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3303-2024·2024-10-09

    Urinalysis reagent strips recalled for reduced protein detection sensitivity

    Healgen Scientific is recalling 1,636,994 urinalysis test strips in California, Georgia, and Texas due to reduced protein detection sensitivity that may produce false negative results and delay kidney disease diagnosis.

    Product
    Healgen Series Reagent strips for Urinalysis are composed of several color pads aligned on a test strip. Each pad is employed for testing one assay item by visually or instrumentally reading the color change of the pad and comparing with the corresponding blocks on a color…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0002-2025·2024-10-09

    Kerala Mixture Snack Recalled for Undeclared Wheat Allergen

    Grace Imports recalled Kerala Mixture snack due to undeclared wheat allergen. The supplier failed to disclose wheat on the product label, posing a risk to consumers with wheat allergies.

    Product
    KERALA MIXTURE INGREDIENTS: Gram Flour 48%, Edible Veg Oil (Refined Palmolein Oil) 36%, Peanuts 6%, Roasted Bengal Gram, Salt 1.5%, Chilly powder 1%, Curry leaf, Asafoetida, Natural Antioxidant (Mixed Tocopherol INS 305) ALLERGEN INFORMATION: Made in a Factory that Process…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0022-2025·2024-10-09

    Cranberry Muffins Recalled for Undeclared Milk and Wheat Allergens

    The Posh Bakery is recalling Cranberry Muffins due to undeclared whey (milk) and wheat flour, as well as missing nutrition facts panel and allergen statement. Consumers with milk or wheat allergies should not consume these products.

    Product
    Whole Grains Bakery labeled "Cranberry Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-3306-2024·2024-10-09

    DVOT SARS-CoV-2 Antigen Test Kit Recalled for Lack of FDA Authorization

    The DVOT SARS-CoV-2 Antigen Test Kit (Model FCY-AGT-01) manufactured by Feng Chun Yuan Medical Equipment has been recalled from the U.S. market because it was not authorized for sale in the United States.

    Product
    DVOT SARS-CoV-2 ANTIGEN TEST KIT, Model Number FCY-AGT-01
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-3307-2024·2024-10-09

    DVOT SARS-CoV-2 and Influenza Antigen Test Kits lack FDA authorization

    The DVOT SARS-CoV-2 & Influenza A+B Antigen Combo Test Kit (Model FAT01) has not obtained FDA authorization for sale in the United States. All lots distributed in the U.S. are subject to recall.

    Product
    DVOT SARS-Cov-2 &Influenza A+B Antigen Combo Test Kit, Model Number FAT01
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0006-2025·2024-10-09

    Ryaltris Nasal Spray Recalled for Clogged Dip Tube

    Ryaltris nasal spray is being recalled because the dip tube is clogged, preventing the spray from functioning. The recall affects 45,504 bottles distributed nationwide.

    Product
    RYALTRIS — RYALTRIS (OLOPATADINE HYDROCHLORIDE AND MOMETASONE FUROATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0002-2025·2024-10-09

    Ciclopirox Gel 0.77% Tubes Recalled Due to Broken Seals

    Glenmark Pharmaceuticals is recalling Ciclopirox Gel 0.77% tubes nationwide due to broken seals. The recall affects 11,568 tubes; no illnesses or injuries have been reported.

    Product
    Ciclopirox Gel 0.77%, For Dermatologic Use Only, Not for Use in Eyes, Rx Only, a) 30 gm Tube, NDC 68462-0455-35; b) 45 gm Tube, NDC 68462-0455-47; c) 100 gm Tube, NDC 68462-0455-94, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa 403513, India, Manufactured…
    Category
    Drug
    Distribution
    Distributed nationwide