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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29926–29950 of 39756

  • SevereFDA (Food)·F-0544-2015·2014-12-03

    MaraNatha Almond Butter Recalled for Potential Salmonella Contamination

    nSpired Natural Foods is recalling MaraNatha No Stir Crunchy Almond Butter due to potential Salmonella contamination. The product was distributed in the US, Canada, and other countries.

    Product
    MaraNatha No Stir Crunchy Almond Butter, 12 oz., UPC 51651093699.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0581-2015·2014-12-03

    Kerry Breakfast Sausage Seasoning Recalled for Salmonella Contamination

    Kerry Foods is recalling 148 bags of Breakfast Sausage Seasoning because an ingredient tested positive for Salmonella.

    Product
    Item Number B18780.01, Kerry Breakfast Sausage Seasoning, Net WT 50 Lb (22.68 KG), Lot Number: 0407424305
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0579-2015·2014-12-03

    Kerry Foods Recalls Sausage Crumble Due to Salmonella Risk

    Kerry Foods is recalling specific lots of Sausage Crumble because an ingredient tested positive for Salmonella.

    Product
    Item Number 30499117.0, Kerry CI 96004320, Sausage Crumble 30499117, 40.05 lbs (18.16 KG) Lot Number : 0401423904
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0261-2015·2014-12-03

    Perry Drug Recalls Tri-Mix Vials Due to Sterility Assurance Concerns

    Perry Drug Inc. is recalling 17 vials of compounded Tri-Mix in Kansas and Missouri due to quality control issues affecting sterility assurance.

    Product
    Tri-Mix (PGE-10MCG/PAP-30MG/PT 5Ml vials, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-5123-09
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0284-2015·2014-12-03

    Hospira Recalls Normosol-R IV Bags Due to Sterility Concerns

    Hospira is recalling 305,664 bags of Normosol-R Multiple Electrolytes Injection due to potential punctures that may compromise sterility and cause leaks.

    Product
    Normosol-R Multiple Electrolytes Injection Type 1, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7967-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0573-2015·2014-12-03

    Karlsburger Foods Recalls Low Sodium Taco Seasoning for Undeclared Milk

    Karlsburger Foods is recalling Low Sodium Taco Seasoning because it contains milk, an allergen not declared on the label.

    Product
    Karlsburger Foods Low Sodium Taco Seasoning, Item Numbers 16423 (Packaged in 23 oz resealable plastic containers), Item #16465 (Packaged in 6.8 lb. resealable plastic containers), and Item #16425 (Packaged in 25 lb. bag in a box).
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Drugs)·D-0276-2015·2014-12-03

    Baxter Recalls Heparin Sodium Injection Due to Low Potency

    Baxter Healthcare is recalling Heparin Sodium in Sodium Chloride Injection because the raw material was found to have low potency.

    Product
    HEPARIN SODIUM IN SODIUM CHLORIDE — HEPARIN SODIUM IN SODIUM CHLORIDE (HEPARIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0263-2015·2014-12-03

    Perry Drug Recalls Phenylephrine Syringes Due to Sterility Concerns

    Perry Drug Inc. is recalling specific lots of compounded Phenylephrine HCl syringes due to quality control issues affecting sterility assurance.

    Product
    Phenylephrine HCl (100 mcg/mL syr) in 0.9% NaCl 1 mg / 10 mL, 3Ml Syringes, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-5230-12
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0270-2015·2014-12-03

    Perry Drug Recalls Human Chorionic Gonadotropin Injections for Sterility Concerns

    Perry Drug Inc. is recalling HCG injections due to quality control issues that may compromise sterility assurance.

    Product
    2Ml HCG 10,000 U/ MB12 - 12,000 MCG/10 Ml Inj, 0.25ML (250IU), Rx, Perry Drug Compounding Pharmacy, Overland Park, KS ---NDC 88888-7945-17
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-0560-2015·2014-12-03

    MaraNatha Peanut Butter Recalled for Potential Salmonella Contamination

    nSpired Natural Foods is recalling MaraNatha No Stir Crunchy Peanut Butter due to potential Salmonella contamination. The product was distributed in the US, Canada, and other countries.

    Product
    MaraNatha No Stir Crunchy Peanut Butter, 500 grams, UPC 51651093415.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0287-2015·2014-12-03

    Hospira Recalls Sterile Water for Injection Due to Sterility Concerns

    Hospira is recalling 153,504 bags of Sterile Water for Injection due to potential punctures that may compromise sterility and cause leaks.

    Product
    Sterile Water for Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7990-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0266-2015·2014-12-03

    Perry Drug Recalls Tri-mix Antidote Syringes Due to Sterility Concerns

    Perry Drug Inc. is recalling Tri-mix Antidote syringes in Kansas and Missouri due to potential sterility assurance issues identified during an FDA inspection.

    Product
    Tri-mix Antidote 10 each Syringes, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-0205-17
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0273-2015·2014-12-03

    Perry Drug Recalls Tri Mix Syringes Due to Sterility Concerns

    Perry Drug Inc. is recalling Tri Mix PF SYR 0.5 mL Inj. syringes in Kansas and Missouri due to potential sterility assurance risks identified during an FDA inspection.

    Product
    Tri Mix PF SYR 0.5 mL Inj., Compounded Rx, 10 each, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-5036-49
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-0554-2015·2014-12-03

    Safeway Almond Butter Recalled for Potential Salmonella Contamination

    nSpired Natural Foods is recalling Safeway Open Nature Creamy Almond Butter Salted due to potential Salmonella contamination. The product was distributed in the US, Canada, and other international locations.

    Product
    Safeway Open Nature Creamy Almond Butter Salted, 12 oz., UPC 79893113746
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0281-2015·2014-12-03

    Hospira Recalls Lactated Ringer's and 5% Dextrose Injection Bags

    Hospira is recalling 275,448 bags of Lactated Ringer's and 5% Dextrose Injection due to potential punctures that may compromise sterility and cause leaks.

    Product
    Lactated Ringer's and 5% Dextrose Injection, USP; 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7929-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0269-2015·2014-12-03

    Perry Drug Recalls HCG Injections Due to Sterility Assurance Concerns

    Perry Drug Inc. is recalling HCG 10,000 U/10 mL PF Inj vials in Kansas and Missouri due to quality control issues affecting sterility assurance.

    Product
    HCG 10,000 U/ 10 mL PF Inj, 8Ml vials, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-5012-34
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0267-2015·2014-12-03

    Perry Drug Recalls HCG Vials Due to Sterility Assurance Concerns

    Perry Drug Inc. is recalling HCG Low Dose vials in Kansas and Missouri due to quality control issues affecting sterility assurance.

    Product
    HCG Low Dose 10 IU / 0.1 mL, 5 Ml vials, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS ---NDC 88888-2596-17
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-0572-2015·2014-12-03

    Karlsburger Foods Taco Seasoning Recalled for Undeclared Milk Allergen

    Karlsburger Foods is recalling specific items of Taco Seasoning because the product contains milk, an allergen not declared on the label.

    Product
    Karlsburger Foods Taco Seasoning, Item Numbers 43823 (Packaged in 23 oz resealable plastic containers), Item #43807 (Packaged in 7 lb. resealable plastic containers), Item #43825 (Packaged in 25 lb. bag in a box), and Item #43850 (Packaged in 50 lb. bag in a box).
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Drugs)·D-0286-2015·2014-12-03

    Hospira Recalls 0.45% Sodium Chloride Injection Due to Sterility Concerns

    Hospira is recalling 784,920 bags of 0.45% Sodium Chloride Injection because punctures in the packaging may compromise sterility and cause leaks.

    Product
    0.45% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7985-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0282-2015·2014-12-03

    Hospira Recalls 5% Dextrose and 0.9% Sodium Chloride Injection Bags

    Hospira is recalling 340,272 bags of 5% Dextrose and 0.9% Sodium Chloride Injection due to potential punctures that may compromise sterility and cause leaks.

    Product
    5% Dextrose and 0.9% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7941-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V770000·2014-12-03

    Chrysler Recalls 2004-2005 Vehicles Due to Air Bag Inflator Rupture Risk

    Chrysler is recalling 2004-2005 Dodge and Chrysler vehicles sold in high-humidity areas because the passenger air bag inflator may rupture during deployment.

    Product
    DODGE — DODGE, CHRYSLER RAM 3500, RAM 2500, MAGNUM, DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0283-2015·2014-12-03

    Hospira Recalls Lactated Ringer's Injection Due to Sterility Concerns

    Hospira is recalling 6,193,416 bags of Lactated Ringer's Injection because potential punctures may compromise sterility and cause leaks.

    Product
    Lactated Ringer's Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7953-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0279-2015·2014-12-03

    Hospira Recalls 5% Dextrose Injection Bags Due to Sterility Concerns

    Hospira is recalling 301,560 bags of 5% Dextrose Injection due to potential punctures that may compromise sterility and cause leaks.

    Product
    5% Dextrose Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7922-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0278-2015·2014-12-03

    Hospira Recalls Potassium Chloride IV Bags Due to Sterility Concerns

    Hospira is recalling 836,460 bags of Potassium Chloride IV solution due to potential punctures that may compromise sterility and cause leaks.

    Product
    Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7902-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0259-2015·2014-12-03

    Perry Drug Recalls Compounded Testosterone Syringes Due to Sterility Concerns

    Perry Drug Inc. is recalling compounded Testosterone CYP-250/PROP-20 mg syringes in Kansas and Missouri due to quality control issues affecting sterility assurance.

    Product
    Testosterone CYP-250/PROP-20 mg, 10 Ml Syringe, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-0326-44
    Category
    Drug
    Distribution
    2 states