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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4851–4875 of 7451

  • CriticalFDA (Food)·F-2235-2015·2015-05-20

    Whole Foods Enchilada Recall for Undeclared Peanut Protein

    Whole Foods Market is recalling Adobo Black Bean Enchiladas due to undeclared peanut protein. Consumers should not eat the product.

    Product
    Enchilada, Adobo Black Bean UPC/PLU: 26735600000
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-2267-2015·2015-05-20

    Aurora Deluxe Mixed Nuts Recalled for Salmonella Risk

    Aurora Products is recalling Deluxe Mixed Nuts with Sea Salt due to a Salmonella risk. The recall covers bulk and 9 oz. cup products distributed in the US and Canada.

    Product
    Deluxe Mixed Nuts with Sea Salt: Aurora, Bulk; Gourmet Garage, 9 oz. Plastic Cup, UPC: 79084505945
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2261-2015·2015-05-20

    Aurora Nut Tray Assortment Recalled Due to Salmonella Risk

    Aurora Products is recalling 6 Section Nut Tray Assortments because of a potential Salmonella contamination. The recall covers specific UPCs and best-by dates.

    Product
    6 Section Nut Tray Assortment: Aurora, 26 oz. Plastic Tray, UPC: 65585200145; Food Emporium Brand, 26 oz. Plastic Tray, UPC: 1119079012
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2262-2015·2015-05-20

    Aurora Cranberry Health Mix Recalled for Salmonella Contamination Risk

    Aurora Products is recalling various Cranberry Health Mix products due to potential Salmonella contamination. The recall covers products sold in the US, Canada, and Bermuda.

    Product
    Cranberry Health Mix: America Choice, 16 oz. Plastic Pouch, UPC: 75480779046; Aurora , 9.25 oz. Plastic Cup, UPC: 65585200288; Aurora , 10.0 oz. Pillow Pouch, UPC: 65585200826; Aurora, 16.0 oz. Plastic Pouch, UPC: 65585200827, Aurora , 18 oz. Plastic Pouch , NO UPC; Aurora , 21…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalNHTSA·15E040000·2015-05-18

    Takata Frontal Driver Air Bag Inflator Module Recall

    Takata is recalling specific frontal driver air bag inflator modules that may rupture during deployment, potentially causing serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0982-2015·2015-05-13

    Physician Preferred Medical Recalls Epel 18 mg Estradiol Pellets Due to Sterility Failure

    Physician Preferred Medical, LLC is recalling Epel 18 mg Estradiol Pellets because the specific lot failed sterility testing. The product was distributed in Arizona and Kansas.

    Product
    Epel 18 mg Estradiol Pellet, For In Office Use Only, For In Office Administration Only, Not for Resale or Dispensing to an Individual Patient, Rx Only, Preferred Physician Medical LLC, 405-551-8216
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Food)·F-2196-2015·2015-05-13

    La Terra Fina Spinach Artichoke Dip Recalled for Listeria Risk

    La Terra Fina is recalling specific lots of Chunky Spinach Artichoke & Parmesan Dip because the chopped spinach ingredient tested positive for Listeria monocytogenes.

    Product
    La Terra Fina Chunky Spinach Artichoke & Parmesan Dip 31-ounce tub Keep refrigerated 31-ounce tub; UPC: 6-40410-51193-4 Item number 407600 - Costco Item number 4300193 - Smart and Final 10 oz. Retail size - UPC 6-40410-51327-3 Manufactured by La Terra Fina, Union…
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Drugs)·D-0977-2015·2015-05-13

    FDA Recalls EDGE Weight Release Capsules Containing Unapproved Drugs

    Detox Transforms is recalling EDGE Amplified Weight Release capsules because the product contains undeclared phenolphthalein and fluoxetine, making it an unapproved drug.

    Product
    EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00417 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0991-2015·2015-05-13

    Ultra ZX Dietary Supplement Recalled for Undeclared Sibutramine and Phenolphthalein

    Ultra ZX Labs is recalling Ultra ZX dietary supplements because FDA testing found undeclared sibutramine and phenolphthalein. The product was marketed without an approved NDA or ANDA.

    Product
    ULTRA ZX DIETARY SUPPLEMENT (Extracto de Naranjo Amargo 70, Extracto de semilla de Sen 47.6, Lagrima de Coix 42, Almidon Medico 84), 30 capsule bottles, Manufactured and distributed by: Ultra ZX Labs, L.L.C. 2525 SW 3rd Ave Apt 1704 Miami, Florida 33129-2068.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0981-2015·2015-05-13

    FDA Recalls iNSANE Bee Pollen Capsules Containing Unapproved Drugs

    The FDA is recalling iNSANE Bee Pollen capsules because they contain undeclared phenolphthalein and fluoxetine, making them unapproved drugs.

    Product
    iNSANE Bee Pollen capsules, 200 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00408 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0994-2015·2015-05-13

    Forever Beautiful Bee Pollen Recalled for Contaminants

    REFA Enterprises is recalling Forever Beautiful Bee Pollen capsules because FDA analysis found the product contains sibutramine and phenolphthalein.

    Product
    Forever Beautiful BEE POLLEN, capsules, 250mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0993-2015·2015-05-13

    REFA Enterprises Recalls Forever Beautiful INFINITY Capsules for Unapproved Ingredients

    REFA Enterprises is recalling Forever Beautiful INFINITY capsules because FDA analysis found the product contains sibutramine and phenolphthalein without an approved NDA/ANDA.

    Product
    Forever Beautiful INFINITY, capsules, 300mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0988-2015·2015-05-13

    FDA Recalls Estrastain Pro-Anabolic Mass and Hardening Complex Capsules

    Anabolic Science Labs LLC is recalling Estrastain Pro-Anabolic Mass and Hardening Complex capsules because they contain unapproved synthetic hormone ingredients.

    Product
    ESTRASTAIN PRO-ANABOLIC MASS AND HARDENING COMPLEX (Estra-4,9,11-triene-3,17-dione 15mg, 2a-3a-epithio-17a-methyl-5a-androstan-17b-ol 10 mg), Capsules, 60 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2194-2015·2015-05-13

    La Terra Fina Spinach Dip Recalled for Listeria Contamination

    La Terra Fina is recalling Organic Thick & Creamy Spinach Dip and Spread because the chopped spinach ingredient tested positive for Listeria monocytogenes.

    Product
    La Terra Fina Organic Thick & Creamy Spinach Dip and Spread; Made with Greek Yogurt. 24 oz. plastic tub (1 lb. 8 oz,) 680 g: Keep refrigerated UPC 640410513730. Manufactured by" La Terra Fina, Union City, CA 94587
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Drugs)·D-0989-2015·2015-05-13

    FDA Recalls Unapproved Anabolic Steroid Supplements from Anabolic Science Labs

    Anabolic Science Labs is recalling SWOLL-250 Super Mass Builder Quad Stack capsules because they contain unapproved synthetic hormone ingredients.

    Product
    SWOLL-250 SUPER MASS BUILDER QUAD STACK (18-Methylestr-4-en-3-one-17b-ol 15mg, 6-a-Chloro-androst-4-en-17b-ol-3-one 15mg, 13-ethyl-3-methoxy-gona-2,5(10)-diene-17-one 15mg, 2,17a-dimethyl-5a-androsta-1-en-17b-ol-3-one 3 mg), Capsules, 90 count bottle, Manufactured for: Wyked…
    Category
    Drug
    Distribution
    Distributed nationwide
  • 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
  • CriticalFDA (Food)·F-2141-2015·2015-05-06

    Red River Foods Recalls Macadamia Nuts Due to Salmonella Risk

    Red River Foods is voluntarily recalling 13,750 lbs of South Africa Macadamia Nuts after a repacker in Texas tested positive for Salmonella.

    Product
    Style 2 South Africa Macadamia Nuts,
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-2082-2015·2015-05-06

    Sabra Classic Hummus Recalled Due to Listeria Monocytogenes Contamination

    Sabra Dipping Company is recalling 10 oz Classic Hummus after a Michigan sample tested positive for Listeria monocytogenes.

    Product
    Sabra Classic Hummus 10 oz UPC 040822011143 / 300067, Sabra Dipping Co. LLC, White Plains, NY
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2120-2015·2015-05-06

    JCB Flavors Recalls Ground Cumin Seasonings Due to Peanut Allergen

    JCB Flavors is recalling various seasonings containing ground cumin because the ingredient tested positive for trace peanut allergens.

    Product
    JCB FLAVORS, LLC, Product Code 4006500812 / 40650/406500812/771756/ 40650, Cumin Ground #400650/40650/44650, 12x 8oz jar, 12x 3.4 oz jar, 12 x 16 oz jar, 1 x 16 oz jar, ,4 x 5 lb jug, bulk ( 25 lb, 10 lb, 2 lb) , UPC: 66049248116, 66049248106, 66049248125, 014641001128…
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-2043-2015·2015-05-06

    Giant Eagle Recalls Iced Cut Out Cookies Due to Undeclared Milk

    Giant Eagle is recalling iced cut out cookies sold in its bakeries because they contain an undeclared milk allergen.

    Product
    All varieties and packaging configurations of iced cut out cookies, labeled as Decorated Cut Out Cookie and Cut Out Cookies, 1oz and 2oz sold individually behind the bakery department service counter, and also pre-packaged in 2 counts (5oz), 10 counts (15oz), inside clear…
    Category
    Food
    Distribution
    4 states