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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5376–5400 of 7463

  • SevereFDA (Food)·F-0224-2023·2023-01-11

    Culvers Tartar Sauce 2 oz Cups Recalled for Undeclared Allergens

    Culvers tartar sauce is being recalled because it contains undeclared fish, soy, and milk allergens. Food service locations should remove the product immediately.

    Product
    Culvers Tartar Sauce 2 oz. plastic cups
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0220-2023·2023-01-11

    Three Gold Coins Dried Mushrooms Recalled for Salmonella Contamination

    Tai Phat Wholesalers LLC is recalling Three Gold Coins Dried Mushrooms due to Salmonella contamination. The product was distributed to multiple states including Florida, New York, and Pennsylvania.

    Product
    Three Gold Coins, Dried Mushrooms (01052) Nam Meo Nguyen Tai S- 50x2.5 oz
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0219-2023·2023-01-11

    Three Gold Coins Dried Mushrooms Recalled Due to Salmonella Contamination

    Three Gold Coins Dried Mushrooms Sliced have been recalled due to Salmonella contamination. Affected product was distributed across 15 U.S. states.

    Product
    Three Gold Coins, Dried Mushrooms Sliced (01276) Nam Meo Soi L- 24x10.5 oz.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0218-2023·2023-01-11

    Three Gold Coins Dried Mushrooms Recalled for Salmonella Contamination

    Three Gold Coins brand dried mushrooms have been recalled due to Salmonella contamination. Approximately 341.2 cases were distributed across 15 U.S. states.

    Product
    Three Gold Coins, Dried Mushrooms Sliced (01051) Nam Meo Soi S- 50x2.5 oz
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0216-2023·2023-01-11

    Power Life Protein Powder Recalled Due to Undeclared Milk

    Power Life High Impact Plant Protein in chocolate flavor is recalled because the product label does not declare milk as an ingredient, creating a serious allergic reaction risk for milk-allergic consumers.

    Product
    Power Life by Tony Horton High Impact Plant Protein Chocolate Flavor NET WT 446 G (15.7 OZ) Ingredients: Vegan Protein Mix (pumpkin, sunflower, flax)(as ProteoSMART), Mung Bean Protein, myHMB (Calcium Beta-hydroxy-Beta-Methlbutyrate), Alkalized Cocoa Powder, Pea Protein Powder,
    Category
    Food
    Distribution
    0 states
  • CriticalCPSC·23088·2023-01-09

    Fisher-Price Recalls 4.7 Million Rock 'n Play Sleepers Due to Infant Deaths

    Fisher-Price is recalling approximately 4.7 million Rock 'n Play Sleepers after at least 8 deaths were reported following the initial April 2019 recall announcement. Infants have died after rolling from their back to their stomach or side while unrestrained.

    Product
    All models of Rock 'n Play Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·23089·2023-01-09

    Kids2 Rocking Sleepers Recalled After 15 Infant Deaths

    Kids2 is recalling approximately 694,000 Rocking Sleepers after 15 infant fatalities were reported. Infants died after rolling from their back to their stomach or side while unrestrained.

    Product
    All models of Kids2 Rocking Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23720·2023-01-05

    Polaris Sportsman and Scrambler 1000 S ATVs recalled for fire hazard

    Polaris is recalling certain 2020–2023 Sportsman and Scrambler 1000 S all-terrain vehicles because electrostatic discharge can ignite fuel during refueling, creating a fire hazard. The company has received 16 reports of fires, including one personal injury.

    Product
    Model Year 2020-2023 Sportsman 1000 S and Scrambler 1000 S All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0208-2023·2023-01-04

    Favorina Advent Calendar recalled for potential Salmonella contamination

    Lidl US Trading is recalling Favorina Advent Calendar due to potential Salmonella contamination. Approximately 10,524 units were distributed throughout the United States.

    Product
    Favorina Advent Calendar NET WT. 8.4OZ (240g) Premium Chocolate with a Creamy Filling UPC 4056489516965
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0212-2023·2023-01-04

    Lukai sweetened jujube products recalled for undeclared sulfites

    Lukai sweetened jujube products are recalled because they contain undeclared sulfites at 17.9 mg per serving. This allergen poses a risk to consumers with sulfite sensitivity.

    Product
    "Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name: Ejiao dates; Ingredients: a nuclear-free golden jujube, donkey-hide gelatin, sugar, honey, maltose, citric acid; Consumption methods: open bags of ready-to-eat, soup, making cakes; Shelf li
    Category
    Food
    Distribution
    13 states
  • SevereCPSC·23083·2022-12-29

    ZLINE Gas Ranges Recalled for Carbon Monoxide Poisoning Risk

    ZLINE is recalling about 28,000 gas ranges because the oven can emit dangerous levels of carbon monoxide while in use, posing a serious risk of injury or death. The firm has received 44 reports of carbon monoxide emission, including three reports of consumers seeking medical attention.

    Product
    ZLINE 30-inch and 36-inch RG gas ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0203-2023·2022-12-28

    Utopia Brand Enoki Mushroom Recalled Due to Listeria Contamination

    Utopia Foods Inc. is recalling Utopia brand Enoki Mushrooms (200g) due to potential Listeria monocytogenes contamination. Consumers should not consume this product.

    Product
    Utopia brand Enoki Mushroom; Utopia Foods Inc; 200g; Product of China; Distributed by Utopia Foods Inc.; UPC 892891861017; packaged in blue and clear plastic bag
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0205-2023·2022-12-28

    Gamesa Arcoiris Marshmallow Cookies recalled due to Salmonella risk

    Gamesa Arcoiris Marshmallow Cookies with best-before date 28MAR23 are being recalled due to potential Salmonella contamination. Approximately 19,764 boxes were distributed in Texas and California.

    Product
    Gamesa Arcoiris Marshmallow Cookies, Naturally and Artificially Flavored 15.5 Oz, 6 Count UPC 6 86700 10132 4
    Category
    Food
    Distribution
    0 states
  • CriticalCPSC·23078·2022-12-22

    Target Recalls Pillowfort Weighted Blankets Due to Asphyxiation Risk

    Target is recalling about 204,000 Pillowfort Weighted Blankets because children can become entrapped inside the blanket cover, creating a risk of asphyxiation. Two children have died from this hazard.

    Product
    Pillowfort™ Weighted Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23080·2022-12-22

    Samsung Top-Load Washing Machines Recalled for Fire Hazard

    Samsung has recalled about 663,500 top-load washing machines because the machines can short-circuit and overheat, posing a fire hazard. A free software update is available to resolve the issue.

    Product
    Samsung Top-Load Washing Machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0438-2023·2022-12-21

    Arrow AC3 Optimus IABP recalled for shortened battery run-times

    Arrow AC3 Optimus Intra-Aortic Balloon Pump (IABP) devices are recalled worldwide due to a potential issue with shortened battery run-times. All lot and serial numbers of model IAP-0700 are affected.

    Product
    Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700 (IPN001112), cardiac pump
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0080-2023·2022-12-21

    FDA Recalls Sodium Bicarbonate Injection Vials for Glass Breakage Risk

    Exela Pharma Sciences is recalling Sodium Bicarbonate Injection vials due to defective containers that may break and release glass fragments when pressurized during preparation. The recall affects 37,320 vials distributed nationwide.

    Product
    8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, Inc. Lehi, Utah 84043, Mfd by: Exela Pharma Sciences, LLC, Lenoir, NC 28645, Carton NDC 72572-740-20, vial NDC 72572-740-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0437-2023·2022-12-21

    Arrow AutoCAT2 Intra-Aortic Balloon Pump Recalled for Short Battery Run-Times

    Arrow International is recalling the AutoCAT2 Intra-Aortic Balloon Pump due to a potential issue with short battery run-times that could affect the device's ability to provide continuous cardiac support.

    Product
    Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601(IPN917288), cardiac pump
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0432-2023·2022-12-21

    Arrow AutoCAT2 Intra-Aortic Balloon Pump Battery Runtime Recall

    The Arrow AutoCAT2 intra-aortic balloon pump has been recalled due to potential short battery run-times. This Class I recall affects devices distributed worldwide.

    Product
    Arrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT2 WAVE REFURBISHED, REF IAP-0535X (IPN000329), cardiac pump
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0455-2023·2022-12-21

    Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump Recalled for Short Battery Run-Times

    Arrow International is recalling Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump devices worldwide due to a potential issue with short battery run-times.

    Product
    Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-05001 (IPN000333), cardiac pump
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0351-2023·2022-12-21

    Arrow MAC Two-Lumen Central Venous Access Kit connector housing defect

    ARROW INTERNATIONAL is recalling Arrow MAC Two-Lumen Central Venous Access Kits due to potential inadequate connection between the top and bottom housings of included Micro Clave Clear Connectors.

    Product
    Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0086-2023·2022-12-21

    Injectable iohexol syringes recalled for mislabeled iodine strength

    BayCare Integrated Service Center is recalling 250 iohexol injection syringes mislabeled as 300 mg iodine/mL but actually containing 350 mg iodine/mL. The labeling error could result in dosing mistakes.

    Product
    Iohexol (300 mg Iodine/mL), 2.4 g Iodine/8 ml, Total Volume 8 ml in 10 ml syringe, 5-count syringes packaged in a bag labeled as Omnipaque (iohexol) 300 mg I/mL, 2.4g Iodine/8 mL in a 10 mL syringe, Compounded with GE Healthcare product, Each mL contains (647 mg) of iohexol as 30
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0433-2023·2022-12-21

    Arrow AutoCAT2 Intra-Aortic Balloon Pump Recalled for Battery Run-Time Issue

    Arrow International is recalling the AutoCAT2 Intra-Aortic Balloon Pump worldwide due to a potential issue with short battery run-times. All lot and serial numbers are affected.

    Product
    Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/EMEA, REF IAP-0600 (IPN001108), cardiac pump
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0441-2023·2022-12-21

    Arrow AC3 Optimus Intra-Aortic Balloon Pumps recalled for short battery runtime

    Arrow International is recalling Arrow AC3 Optimus Intra-Aortic Balloon Pumps worldwide due to a potential issue with short battery run-times. The pumps may not operate for the intended duration during critical cardiac care.

    Product
    Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/AJLA, REF IAP-0701 (IPN001113), cardiac pump
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0444-2023·2022-12-21

    Arrow AutoCAT 2 Intra-Aortic Balloon Pump Short Battery Runtime Recall

    Arrow International is recalling the Arrow AutoCAT 2 Intra-Aortic Balloon Pump (IABP) due to a potential issue with short battery run-times. The recall affects 29 units distributed worldwide.

    Product
    Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400E (IPN000305), cardiac pump
    Category
    Medical Device
    Distribution
    0 states