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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27951–27975 of 39756

  • CriticalFDA (Food)·F-2153-2015·2015-05-13

    Spiceco Recalls Hungarian Paprika Due to Undeclared Peanut Protein

    Spiceco is recalling Pride of Szeged Sweet Hungarian Paprika because it may contain undeclared peanut protein. The recall includes additional products containing the implicated paprika.

    Product
    Pride of Szeged Hungarian Exquisite 100 % Sweet Delicacy Paprika, Net Wt. 5 oz., 142g, UPC 0 78006 00010 2
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0979-2015·2015-05-13

    AMPD GOLD Bee Pollen Recalled for Undeclared Sildenafil

    Detox Transforms is recalling AMPD GOLD Bee Pollen capsules because they contain undeclared sildenafil, making them unapproved drugs.

    Product
    AMPD GOLD Bee Pollen capsules, 350 mg, 60-count bottle, Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00418 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0986-2015·2015-05-13

    FDA Recalls Unapproved Anabolic Steroid Product HALO-70 MEGA MASS BUILDER

    The FDA is recalling HALO-70 MEGA MASS BUILDER capsules because they contain an unapproved synthetic hormone ingredient, making them unapproved new drugs.

    Product
    HALO-70 MEGA MASS BUILDER (4-chloro-17a-methyl-androst-1,4-diene-3b,17b-diol 35mg), Capsules, 60 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0978-2015·2015-05-13

    Detox Transforms Recalls iNDiGO Capsules Containing Undeclared Phenolphthalein

    Detox Transforms is recalling iNDiGO capsules because they contain undeclared phenolphthalein, making the product an unapproved drug.

    Product
    iNDiGO capsules, 220 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00404 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V286000·2015-05-13

    Toyota Recalls Vehicles for Front Passenger Air Bag Inflator Rupture Risk

    Toyota is recalling specific 2002-2007 Lexus, Toyota, and Pontiac vehicles because the front passenger air bag inflator may rupture during a crash, potentially causing serious injury or death.

    Product
    PONTIAC — PONTIAC, LEXUS, TOYOTA VIBE, SC, SEQUOIA, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0985-2015·2015-05-13

    FDA Recalls M14-Ment Advanced Mass Builder for Unapproved Steroid Ingredient

    The FDA is recalling M14-Ment Advanced Mass Builder capsules because they contain an unapproved synthetic hormone ingredient, making them unapproved new drugs.

    Product
    M14-MENT ADVANCED MASS BUILDER (7a-Methyl-estra-4-en-3,17-dione MENT 5mg, M14D 20 mg), Capsules, 90 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2147-2015·2015-05-13

    Royal Frozen Food Recalls Blintzes with Cherry Due to Undeclared Milk

    Royal Frozen Food is recalling Blintzes with Cherry because the product contains undeclared milk. The recall affects 3,600 units distributed in California and Nevada.

    Product
    Blintzes with Cherry, Net Wt. 18oz (510g), 10 pieces. 18-oz. plastic trays containing ten pieces of Royal Frozen Food, BLINTZES Blintzes with Cherry with bar code 6 0723830021 8; 12 packs per case.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0976-2015·2015-05-13

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Human Hair

    Hospira Inc. is recalling 9,912 units of 0.9% Sodium Chloride Injection, USP, 250 mL, because human hair was found floating in the IV solution.

    Product
    0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2148-2015·2015-05-13

    Royal Frozen Food Recalls Blintzes with Potato for Undeclared Milk

    Royal Frozen Food is recalling Blintzes with Potato because they contain undeclared milk. The recall affects 3,600 units distributed in California and Nevada.

    Product
    Blintzes with Potato, Net Wt. 18oz (510g), 10 pieces. 18-oz. plastic trays containing ten pieces of Royal Frozen Food, BLINTZES Blintzes with Potato with bar code 6 0723830020 1; 12 packs per case.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2169-2015·2015-05-13

    International Foodsource Recalls Ground Cumin Due to Peanut Protein

    International Foodsource, LLC is recalling ground cumin that may contain peanut protein. The product was distributed in Illinois, Massachusetts, Maryland, and Virginia.

    Product
    Ground Cumin, Bulk Package Size: a) 50 lb. paper carton b) 16 oz. jar/ 8 plastic jars per case
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·15V283000·2015-05-13

    Forest River Recalls 2014-2015 Glaval Transit Buses for Loose Tie Rod Nut

    Forest River is recalling 226 model year 2014-2015 Glaval transit buses because a loose tie rod jam nut may cause loss of control.

    Product
    GLAVAL BUS — GLAVAL BUS UNIVERSAL, LEGACY, TITAN II, TITAN II LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V284000·2015-05-13

    Toyota Recalls 2004-2005 RAV4 Vehicles Due to Air Bag Defect

    Toyota is recalling 2004-2005 RAV4 vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of serious injury or death.

    Product
    TOYOTA — TOYOTA RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2195-2015·2015-05-13

    La Terra Fina Spinach Artichoke Dip Recalled for Listeria Risk

    La Terra Fina is recalling Spinach Artichoke & Parmesan Dip made with Greek Yogurt because a supplier notified the firm that the product contained IQF chopped spinach that tested positive for Listeria Monocytogenes.

    Product
    La Terra Fina Spinach Artichoke & Parmesan Dip made with Greek Yogurt 31-ounce tub Keep refrigerated UPC 6-40410-51338-9 Manufactured by" La Terra Fina, Union City, CA 94587
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-2151-2015·2015-05-13

    Wawa Kale and Quinoa Salad Recalled for Undeclared Soy Allergen

    Taylor Farms Florida is recalling Wawa brand Kale and Quinoa Salad because the packaging fails to declare soy as an ingredient.

    Product
    Wawa brand Kale and Quinoa Salad, 7.5-oz. plastic container, UPC Code: 726191066402
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-2145-2015·2015-05-13

    Ossie's Pickled Lox Recalled for Undeclared Milk Allergen

    SM Fish Corp is recalling Ossie's Pickled Lox Dairy due to undeclared milk. The product was distributed in New York and New Jersey.

    Product
    OSSIE'S PICKLED LOX DAIRY, NET WT. 8 OZ, UPC 739885114136 --- The product is packaged in clear, plastic containers/tubs.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2173-2015·2015-05-13

    Giant Eagle Store-Cut Fontal Cheese Recalled for Undeclared Egg Allergen

    Giant Eagle is recalling store-cut Fontal cheese because it contains lysozyme, an egg allergen, that was not declared on the label.

    Product
    Giant Eagle Store cut Fontal Cheese wrapped in plastic wrap Belgium Imported Fontal - CD; Sell By: (up to and including) 04/23/2015 PLU: 16124 Giant Eagle Distributed by: Giant Eagle, Inc., Pittsburgh, PA 15238
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·15V281000·2015-05-13

    Autocar Recalls Xpert and XSpotter Vehicles for Engine Fire Risk

    Autocar is recalling 2014-2016 Xpert and XSpotter vehicles because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    AUTOCAR — AUTOCAR XSPOTTER, XPERT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2150-2015·2015-05-13

    Deer Brand Golden Raisins Recalled for Undeclared Sulfites

    Best Foods NJ, Inc. is recalling Deer Brand Golden Raisins because they contain undeclared sulfites, a potential allergen.

    Product
    Deer Raisin Golden 7 oz., marked and unmarked packages Packed for Best Foods Inc. Edison, NJ 08817 Some have UPC 714760029255. packaged in clear plastic packages.
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·15V285000·2015-05-13

    Toyota Recalls Vehicles for Defective Passenger Air Bag Inflators

    Toyota is recalling approximately 1.97 million vehicles, including Pontiac, Lexus, and Toyota models, to replace passenger air bag inflators that may rupture.

    Product
    TOYOTA — TOYOTA, PONTIAC, LEXUS COROLLA MATRIX, VIBE, SC, SEQUOIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V280000·2015-05-13

    Autocar Recalls Xpeditor Vehicles Due to Engine Fire Risk

    Autocar is recalling 2008-2016 Xpeditor vehicles because a vent tube may detach, allowing engine oil to contact hot surfaces and increase the risk of a vehicle fire.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2149-2015·2015-05-13

    Royal Frozen Food Recalls Blintzes with Potato and Mushroom Due to Undeclared Milk

    Royal Frozen Food is recalling Blintzes with Potato & Mushroom because they contain undeclared milk. The recall affects 3,600 units distributed in California and Nevada.

    Product
    Blintzes with Potato & Mushroom, Net. Wt. 18oz (510g), 10 pieces. 18-oz. plastic trays containing ten pieces of Royal Frozen Food, BLINTZES Blintzes with Potato Mushroom with bar code 6 0723830020 1. 12 packs per case.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2146-2015·2015-05-13

    Ossie's Pickled Lox Recalled for Undeclared Egg Allergen

    SM Fish Corp is recalling Ossie's Pickled Lox & Cream because it contains undeclared eggs, a sub-ingredient of the mayonnaise.

    Product
    OSSIE'S PICKLED LOX & CREAM, NET WT. 8 OZ, UPC 739885114136 --- The product is packaged in clear, plastic containers/tubs.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0984-2015·2015-05-13

    FDA Recalls M1-Alpha Labs Mega Mass Builder for Unapproved Steroid Ingredient

    The FDA is recalling M1-Alpha Labs Mega Mass Builder capsules because they contain an unapproved synthetic hormone ingredient, making them unapproved new drugs.

    Product
    M1-ALPHA LABS MEGA MASS BUILDER (M1A, Methyl-1-Etiocholenolol- 20mg, Epietiocholanolone) Capsules, 60 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0987-2015·2015-05-13

    FDA Recalls 7-Ment Alpha Advanced Mass Builder for Unapproved Steroid Ingredient

    The FDA is recalling 7-Ment Alpha Advanced Mass Builder capsules because they contain an unapproved synthetic hormone ingredient.

    Product
    7-MENT ALPHA ADVANCED MASS BUILDER (7a-methyl-estra-4-en-3,17-dione 10 mg), Capsules, 90 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide