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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34676–34700 of 39756

  • CriticalFDA (Food)·F-1462-2013·2013-06-05

    Whole Foods Peanut Butter Chocolate Chunk Cookies Recalled for Salmonella Risk

    The Sourdough: A European Bakery Inc. is recalling Whole Foods peanut butter chocolate chunk cookies because they were made with peanut butter recalled for salmonella.

    Product
    Whole Foods 3 oz Peanut Butter Chocolate Chunk Cookies sold under PLU 47963 from the retail store self-serve pastry case.
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1449-2013·2013-06-05

    Pecan Deluxe Peanut Butter Crunch Recalled for Salmonella Risk

    Pecan Deluxe Candy Company is recalling Peanut Butter Crunch because it was made with peanut butter previously recalled for salmonella.

    Product
    Peanut Butter Crunch, 45 lb Case, Item Number 01-326-45, Manufactured by Pecan Deluxe Candy Company, 2570 Lone Star Drive, Dallas, TX 75212
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-1450-2013·2013-06-05

    Pecan Deluxe Peanut Butter Fudge Ribbon Recalled for Salmonella Risk

    Pecan Deluxe Candy Company is recalling Peanut Butter Fudge Ribbon because it was made with peanut butter previously recalled for salmonella.

    Product
    Peanut Butter Fudge Ribbon, 50 lb Pail, Item Number 07-094-50, Manufactured by Pecan Deluxe Candy Company, 2570 Lone Star Drive, Dallas, TX 75212
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-1465-2013·2013-06-05

    Arthur Schuman Grated Grana Padano Cheese Recalled for Listeria

    Arthur Schuman Midwest LLC is recalling specific lots of grated Grana Padano cheese because testing found Listeria monocytogenes.

    Product
    GRATED 2/25 GRANA PADANO; Lot Code: 313701A01; Pack Size: 2/25#; Net Pounds: 50; PACK DATE: 05/18/13; ITEM#DGP03; arthur schuman inc, 40 new dutch lane fairfield nj 07004 U.S.A.; 937-227-0030 www.arthurschuman.com;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-495-2013·2013-06-05

    Nora Apothecary Recalls Pyridoxine Injections Due to Sterility Concerns

    Nora Apothecary and Alternative Therapies, Inc. is recalling Pyridoxine 100mg/ml Injections due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    Pyridoxine 100mg/ml Inj MDV, 1X30 ml 30 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-454-2013·2013-06-05

    Nora Apothecary Recalls Bimix Inj 30:0.5 MDV Penile Injection

    Nora Apothecary and Alternative Therapies, Inc. is recalling Bimix Inj 30:0.5 MDV Penile Injection due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    Bimix Inj 30:0.5 MDV, 5 ml syr Penile Injection, 90 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-481-2013·2013-06-05

    Nora Apothecary Recalls Hydroxycobalamin Injections Due to Sterility Concerns

    Nora Apothecary is recalling Hydroxycobalamin Injections because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Hydroxycobalamin Inj 1 mcg/ml MDV, 2x30ml Subcutaneous, 90 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-461-2013·2013-06-05

    Nora Apothecary Recalls Trimix Penile Injection Due to Sterility Concerns

    Nora Apothecary is recalling Trimix penile injections because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Trimix Inj 30:1:10 MDV, 5 ml Penile Injection, 30 and 90 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-470-2013·2013-06-05

    Nora Apothecary Recalls Tobramycin Ophthalmic Solution Due to Sterility Concerns

    Nora Apothecary and Alternative Therapies, Inc. is recalling Tobramycin Ophthalmic Solution due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    Tobramycin Opth Soln 14mg/ml, 7ml Opthalmic Soln, 10 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-457-2013·2013-06-05

    Nora Apothecary Recalls PGE-1 Penile Injections Due to Sterility Concerns

    Nora Apothecary is recalling PGE-1 Penile Injections because FDA inspections raised concerns about quality control and the assurance of sterility.

    Product
    PGE-1 Inj 10mcg/ml MDV, 5ml Penile Injection, 90 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-477-2013·2013-06-05

    FDA Recalls HCG Injections Due to Sterility Concerns

    Nora Apothecary and Alternative Therapies, Inc. is recalling HCG Inj 1200un/ml MDV products due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    HCG Inj 1200un/ml MDV, 10 ml Subcutaneous, 30 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-463-2013·2013-06-05

    Nora Apothecary Recalls Trimix Penile Injections Due to Sterility Concerns

    Nora Apothecary is recalling Trimix penile injections because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Trimix Inj 30:1:40 MDV, 5 ml Penile Injection, 30 and 90 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-490-2013·2013-06-05

    Gentamicin Irrigation Recalled Due to Sterility Assurance Concerns

    Nora Apothecary is recalling Gentamicin 24mg/60ml Irrigation because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Gentamicin 24mg/60ml Irrigation, 15x60ml Syr Irrigation, 14 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-492-2013·2013-06-05

    Nora Apothecary Recalls M.I.C.+B12 Injections Due to Sterility Concerns

    Nora Apothecary and Alternative Therapies, Inc. is recalling M.I.C.+B12 Inj MDV products due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    M.I.C.+B12 Inj MDV: 3x50ml, 4x50 ml 90 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1372-2013·2013-06-05

    AsthmaNefrin Starter Kit Recalled for Choking Hazard

    Nephron Pharmaceuticals is recalling AsthmaNefrin Starter Kits because a component may dislodge and cause a choking hazard.

    Product
    AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one (1) EZ Breathe Atomizer. For the delivery of liquid medications for respiratory usage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-455-2013·2013-06-05

    Nora Apothecary Recalls Bimix Inj Penile Injection Due to Sterility Concerns

    Nora Apothecary is recalling Bimix Inj 30:1 MDV penile injections because FDA inspections raised concerns about quality control and sterility assurance.

    Product
    Bimix Inj 30:1 MDV: 5ml, 10 ml, 3x10ml, 2x10ml Penile Injection, 30 and 90 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-484-2013·2013-06-05

    Nora Apothecary Recalls Methylcobalamin Injections Due to Sterility Concerns

    Nora Apothecary and Alternative Therapies, Inc. is recalling Methylcobalamin Injections due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    Methylcobalamin Inj 5mg/ml MDV: 5 ml, 10 ml, 12 ml, 20 ml Subcutaneous, 90 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-460-2013·2013-06-05

    Nora Apothecary Recalls PGE-1 Penile Injections Due to Sterility Concerns

    Nora Apothecary is recalling PGE-1 Penile Injections because FDA inspections raised concerns about quality control and assurance of sterility.

    Product
    PGE-1 Inj 40mcg/ml MDV, 5 ml Penile Injection, 90 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-469-2013·2013-06-05

    Nora Apothecary Vancomycin Ophthalmic Solution Recalled for Sterility Concerns

    Nora Apothecary is recalling Vancomycin Ophthalmic Solution due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    Vancomycin Opth Soln14mg/ml PF, 10ml Opthalmic Soln, 30 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-479-2013·2013-06-05

    Nora Apothecary Recalls HCG Injections Due to Sterility Concerns

    Nora Apothecary and Alternative Therapies, Inc. is recalling HCG Inj 500un/ml MDV, 5 ml Subcutaneous due to FDA inspection findings regarding quality control and lack of assurance of sterility.

    Product
    HCG Inj 500un/ml MDV, 5 ml Subcutaneous, 30 day expiration,
    Category
    Drug
    Distribution
    Distributed nationwide