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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776–800 of 5642

  • SevereFDA (Drugs)·D-0012-2025·2024-10-23

    Atovaquone Oral Suspension Recalled for Cohnella Bacteria Contamination

    Bionpharma Inc. is recalling Atovaquone Oral Suspension (750 mg/5 mL) nationwide due to Cohnella bacteria contamination. The recall affects 1,980 bottles.

    Product
    ATOVAQUONE — ATOVAQUONE (ATOVAQUONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0043-2025·2024-10-23

    Seasoned Radish Recalled for Undeclared Crustacean Allergen

    Lemonland Food Corp is recalling Item FLD1080A Seasoned Radish due to undeclared shrimp. The product was distributed in Washington; consumers with crustacean allergies should not consume it.

    Product
    Item FLD1080A, Seasoned Radish, distributed in plastic clamshell containers, net wt. 0.365lb. The H-Mart label declares: Radish, Red Pepper Powder, Malt Syrup, Salt, Anchovy, Sugar, Garlic, Ginger, Sesame.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0036-2025·2024-10-23

    Enjoy Premium Coconut Cookies Recalled for Undeclared Milk Allergen

    KTM Services, Inc. is recalling Enjoy Premium Coconut Cookies sold in Hawaii, Guam, Nevada, and online due to undeclared milk allergen. Consumers with milk allergies should not consume the product.

    Product
    Enjoy Premium Coconut Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear bags
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0044-2025·2024-10-23

    Seasoned Dandelion Recalled for Undeclared Fish Allergen

    Lemonland Food Corp is recalling Item FLD1070A Seasoned Dandelion due to undeclared fish (anchovy) not listed on the label. Consumers with fish allergies should not consume this product.

    Product
    Item FLD1070A, Seasoned Dandelion, distributed in plastic clamshell containers. Net wt. 0.365lb. The H-Mart label declares: Dandelion, Salt, Garlic, Soy Sauce, Chili Powder.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0046-2025·2024-10-23

    Octopus Product Recalled for Undeclared Fish Allergen

    Lemonland Food Corp is recalling Item FLD2011 Salted and Seasoned Small Octopus because it contains undeclared fish (anchovy), a major allergen. Approximately 70 packages were distributed in Washington state.

    Product
    Item FLD2011, Salted and Seasoned Small Octopus, distributed in plastic clamshell containers, net wt. 0.267lb. The H-Mart label declares: Octopus, Salt, Garlic, Ginger, Red Pepper Powder, Green Onion, Syrup, Sesame Seed.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0047-2025·2024-10-23

    GE HealthCare Giraffe OmniBed neonatal incubator door screw may loosen

    Certain GE HealthCare Giraffe OmniBed and Carestation neonatal incubators may have door-securing screws that were not torqued to specification, potentially causing the doors to become loose. These units are distributed worldwide.

    Product
    GE Heathcare Giraffe OmniBed; neo natal incubator
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0041-2025·2024-10-23

    Perilla Leaves in Soy Sauce recalled for undeclared wheat and fish allergens

    Lemonland Food Corp recalls Item FLD1000BA Perilla Leaves in Soy Sauce due to undeclared wheat and fish allergens on the label. Consumers with these allergies should not consume the product.

    Product
    Item FLD1000BA, Perilla Leaves in Soy Sauce, distributed in plastic clamshell containers, net wt. 0.315lb. The H-Mart label declares: Perilla Leaves, Soy Sauce, Sugar
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0037-2025·2024-10-23

    Nuts.com recalls S'mores Bites for undeclared milk allergen

    Nuts.com is recalling S'mores Bites due to undeclared milk allergen. Milk chocolate was listed in the product description but omitted from the ingredient list, creating a labeling mismatch.

    Product
    S'mores Bites, 1 yummy pound, Distributed by Nuts.com, Cranford, NJ, 07016
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0048-2025·2024-10-23

    Seasoned Pepper with Soybean Paste Recalled for Undeclared Allergens

    Lemonland Food Corp is recalling Item FLD1020A Seasoned Pepper with Soybean Paste due to undeclared wheat, fish, and crustacean allergens. Consumers with allergies should not consume this product.

    Product
    Item FLD1020A, Seasoned Pepper with Soybean Paste, distributed in plastic clamshell containers. Net wt. 0.315lb. The H-Mart label declares: Pepper, Soy Bean Paste.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0035-2025·2024-10-23

    Enjoy Premium Taro Cookies recalled for undeclared milk allergen

    Enjoy Premium Taro Cookies contain undeclared milk allergen and were sold in Hawaii, Guam, and Nevada. Consumers with milk allergies should not consume this product.

    Product
    Enjoy Premium Taro Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear bags
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0038-2025·2024-10-23

    Potato Salad Recall: Undeclared Egg and Soybean Allergens

    Lemonland Food Corp is recalling potato salad due to undeclared egg and soybean allergens present in the mayonnaise ingredient. The recall affects 120 packages distributed in Washington.

    Product
    Item FLD4006, Potato Salad, distributed in plastic clamshell containers, net wt. 0.56lb. The H-Mart label declares: Potato, Mayonnaise, Sugar, Vegetable.
    Category
    Food
    Distribution
    1 state
  • SevereCPSC·25015·2024-10-17

    Colsen Fire Pits Recalled for Burn Injury Risk from Flame Jetting

    Colsen-branded tabletop fire pits are being recalled due to the risk of invisible alcohol flames causing flame jetting and fire spreading. The hazard can cause serious burns in less than one second.

    Product
    Colsen-branded fire pits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25011·2024-10-17

    Anker Power Banks Recalled for Fire and Burn Hazards

    Anker power banks with model numbers A1642, A1647, and A1652 have been recalled because the lithium-ion battery can overheat and catch fire, causing burn injuries. The firm has received 28 reports of overheating and fires, with two burn injuries reported.

    Product
    Anker Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0005-2025·2024-10-16

    Z-800 Infusion System Recalled for Air-in-Line Software Algorithm Defect

    Zyno Medical LLC is recalling the Z-800 Infusion System due to a defect in the air-in-line software algorithm. Approximately 34,994 units distributed nationwide are affected by this Class I FDA recall.

    Product
    Z-800 Infusion System, Model Numbers Z-800, Z-800F, Z-800W, Z-800WF; Software Version: Z-800 6.1.01 and 6-1.07z; Z-800F 4.1.02 and 4.1.08z; Z-800W 3.1.32 and 3.1.64z, Z-800WF 3.1.32 and 3.1.64z
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0023-2025·2024-10-16

    7-Eleven Fudge Brownies Recalled Due to Undeclared Walnuts

    Innovation Bakers has recalled 7-Eleven Fudge Brownies with Chocolate Chip due to undeclared walnuts. The product was distributed to Southern California 7-Eleven stores and may cause allergic reactions in consumers with walnut allergies.

    Product
    7-Eleven Fudge Brownie with Chocolate Chip, 3.5 oz. UPC: 05254856392
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0008-2025·2024-10-16

    Vail-Bon Jie Yang Wan capsules recalled for undeclared pharmaceutical ingredients

    Vail-Bon Jie Yang Wan capsules have been recalled for containing undeclared dexamethasone and chlorpheniramine. The product was marketed without FDA approval.

    Product
    Vail-Bon Jie Yang Wan capsules, 30-count bottle, Vall Boon Medical Factory Sdn. Bhd., No 1, Lorong Mengkudu, Taman Mengkudu, 14100 Juru, Malaysia.
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·23V905000·2024-10-12

    Ford vehicles recalled for oil pump belt failure and power braking loss

    Certain 2016-2018 Ford Focus and 2018-2022 Ford EcoSport vehicles may have faulty oil pump drive belts or tensioners that can fail, causing engine stall and loss of power braking assist, increasing crash risk.

    Product
    FORD — 2022 FORD ECOSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·25009·2024-10-10

    Fisher-Price Recalls 2.1 Million Snuga Infant Swings for Suffocation Risk

    Fisher-Price is recalling approximately 2.1 million Snuga Infant Swings due to suffocation hazard when the product is used for sleep or bedding is added. Five deaths have been reported between 2012 and 2022.

    Product
    All Models of Fisher-Price Snuga Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1838-2024·2024-10-09

    Kandy brand whole cantaloupes recalled for possible Salmonella contamination

    Eagle Produce LLC is recalling Kandy brand whole cantaloupes due to possible Salmonella contamination. The recalled product (224 cases of 9-count boxes) was distributed to Michigan, Missouri, Ohio, Texas, and Virginia.

    Product
    Whole cantaloupe, brand name Kandy, packed in a corrugated box, 9 count
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0002-2025·2024-10-09

    MiniMed Insulin Pumps Recalled for Battery Failure After Physical Impact

    MiniMed insulin pumps are recalled because physical impact can damage internal components, reduce battery life, and cause unexpected device shutdown that interrupts insulin delivery.

    Product
    MiniMed 620G Insulin Pump, REF: MMT-1510, MMT-1710, MMT-1750; MiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714, MMT-1715, MMT-1754, MMT-1755; MiniMed 640G Insulin Pump, REF: MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1751, MMT-1752; MiniMed 720G Insulin Pump, REF: MMT-1809,
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Devices)·Z-0001-2025·2024-10-09

    MiniMed Insulin Pumps Recalled for Battery Depletion and Delivery Risk

    Medtronic MiniMed 630G and 700G insulin pumps may experience battery depletion and device shutdown after physical impact, interrupting insulin delivery in diabetic patients.

    Product
    MiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714, MMT-1715, MMT-1754, MMT-1755; MiniMed 700G Insulin Pump, REF: MMT-1800, MMT-1801, MMT-1805, MMT-1850, MMT-1851
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Devices)·Z-3207-2024·2024-10-09

    Percussionaire IPV In-Line Valve Recall: Blue Cap Removal Labeling Update

    Percussionaire is recalling the P5-TEE IPV in-line valve to update labeling and ensure the blue cap is removed before use and delivery of the device.

    Product
    Percussionaire, Inc., REF: P5-TEE, Qty: 1, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1837-2024·2024-10-09

    Chicken and Duck Eggs Recalled for Potential Salmonella Contamination

    Milo's Poultry Farms is recalling chicken and duck eggs sold in foodservice and consumer packages in Illinois, Michigan, and Wisconsin due to potential Salmonella contamination.

    Product
    Grade A Brown Chicken Eggs, in shell, Bulk 15 dozen. For Foodservice. Keep Refrigerated. Sold with the following brands: 1. Milo's Poultry Farms, N 3873 Valley Road, Bonduel, WI 54107. Organic Eggs from Free Range Hens. 2. M&E Family Farms, Eggs from Free Range Hens. N
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0004-2025·2024-10-09

    Gold Hard Steel Plus Liquid recalled for undeclared acetaminophen and sildenafil

    FDA has recalled Gold Hard Steel Plus Liquid because the product was marketed without FDA approval and contains undeclared pharmaceutical ingredients: acetaminophen and sildenafil.

    Product
    Gold Hard Steel Plus Liquid, 2 FL OZ bottles, UPC 787188873199
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0005-2025·2024-10-09

    FDA Recalls Veklury Injection Vials for Presence of Glass Particles

    Gilead Sciences recalls 105,000 vials of Veklury (remdesivir) for injection nationwide because glass particles are present in the medication.

    Product
    VEKLURY — VEKLURY (REMDESIVIR)
    Category
    Drug
    Distribution
    Distributed nationwide