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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8626–8650 of 17974

  • SevereFDA (Drugs)·D-0885-2019·2019-03-20

    King Bio Recalls Dr. King's SafeCare Rx Smoke Control Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Smoke Control bottles due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Smoke Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955303022, NDC 57955-3031-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0828-2019·2019-03-20

    FDA Recalls Dr. King's SafeCare Rx Female Enhancer Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Female Enhancer due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Female Enhancer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955011521, NDC 57955-0115-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0727-2019·2019-03-20

    King Bio Recalls Asthma Clear Allergy Spray Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Asthma Clear Allergy nasal spray due to microbial contamination. The affected product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Asthma Clear Allergy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955004424, NDC 57955-0044-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0830-2019·2019-03-20

    King Bio Recalls Allergy Homeopathic Product Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Allergies: Dairy due to potential microbial contamination that could pose a health risk.

    Product
    Dr. King's SafeCare Rx Allergies: Dairy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955219828, NDC 57955-2198-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0951-2019·2019-03-20

    King Bio Recalls NET Remedies Homeopathic Liquid Due to Microbial Contamination

    King Bio Inc. is recalling NET Remedies #10 Scars-Adhesions Homeopathic Preparation due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    NET Remedies #10 Scars-Adhesions Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4210-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0746-2019·2019-03-20

    King Bio Recalls Dr. King's SafeCare Rx Snore Control Sleep

    King Bio Inc. is recalling Dr. King's SafeCare Rx Snore Control Sleep due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Snore Control Sleep, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955012023, NDC 57955-0120-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0541-2019·2019-03-20

    FDA Recalls King Bio Homeopathic Liver Detox Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Liver Detox due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Liver Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955006220, NDC 57955-5062-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0546-2019·2019-03-20

    King Bio Homeopathic Nuts & Seeds Intolerances Recalled for Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Nuts & Seeds Intolerances due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Nuts & Seeds Intolerances, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955520528, NDC 57955-5205-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0923-2019·2019-03-20

    King Bio Inc. Recalls NET Remedies #7 Homeopathic Preparation Due to Microbial Contamination

    King Bio Inc. is recalling NET Remedies #7 Homeopathic Preparation, Oral Liquid, 57 mL, due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    NET Remedies #7 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0712-2019·2019-03-20

    King Bio Recalls Colds and Flu Immune Syrup Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Colds & Flu Immune syrup due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Colds & Flu Immune, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955038221, NDC 57955-0382-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0724-2019·2019-03-20

    King Bio Recalls Indecision Mind & Body Due to Microbial Contamination

    King Bio Inc. is recalling 22 bottles of Dr. King's SafeCare Rx Indecision Mind & Body due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Indecision Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955277026, NDC 57955-2771-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0883-2019·2019-03-20

    King Bio Recalls Dr. King's SafeCare Rx Procrastination Due to Microbial Contamination

    King Bio Inc. is recalling 95 bottles of Dr. King's SafeCare Rx Procrastination because the product contains microbial contamination.

    Product
    Dr. King's SafeCare Rx Procrastination, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955276029, NDC 57955-2761-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0583-2019·2019-03-20

    Dr. King's Natural Medicine Homeopathic Foul Bowel is recalled due to microbial contamination.

    An FDA drug recall affects Dr. King's Natural Medicine Homeopathic Foul Bowel because microbial contamination was detected. Consumers should stop using the product immediately.

    Product
    Dr. King's Natural Medicine Homeopathic Foul Bowel, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955531920, NDC 57955-5319-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1002-2019·2019-03-20

    Roberts Home Medical Recalls Refrigerated Liquid Oxygen Cylinders Due to CGMP Deviations

    Roberts Home Medical LLC is voluntarily recalling 9 refrigerated liquid oxygen reservoirs due to Current Good Manufacturing Practice (CGMP) deviations. The product was distributed in Maryland, Virginia, and the District of Columbia.

    Product
    Oxygen, Refrigerated Liquid USP, Rx only, cylinder, a) Roberts Home Medical, Inc. Rockville MD 20855, b) Roberts Home Medical, Inc. Germantown, MD. 20875
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0996-2019·2019-03-20

    Lannett Recalls Oxybutynin Chloride Tablets for Dissolution Failures

    Lannett Company Inc. is recalling 14,448 bottles of Oxybutynin Chloride Extended-Release Tablets because they failed to meet dissolution specifications.

    Product
    OXYBUTYNIN CHLORIDE — OXYBUTYNIN CHLORIDE (OXYBUTYNIN CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1012-2019·2019-03-20

    Medtech Recalls Little Remedies New Baby Essentials Kit for Labeling Errors

    Medtech Products is recalling 4,716 Little Remedies New Baby Essentials Kits because the cartons contain incorrect labeling for two of the five items inside.

    Product
    Little Remedies New Baby Essentials Kit. Each kit contains 1 each of the following products: Little Remedies Infant Fever Reducer (acetaminophen 150mg) 2 fl. oz. bottle, Little Remedies Saline Spray/Drops (sodium chloride) 0.5 fl oz., Little Remedies Gripe Water (zingiber officin
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1004-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed blend uniformity specifications. The recall covers 140,589 bottles distributed nationwide.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets, USP 80mg/12.5 mg, 30-coun bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Imachal Pradesh, India NDC 33342-129-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1003-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed blend uniformity specifications.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets 40mg/12.5 mg, 30-count bottles, Rx Only, Manufactured for:Macleods Pharma USA, Inc. Plainsboro, NJ 08536, Manufactured for: Macleods Pharmaceuticals Ltd. Baddi, Himchal Pradesh INDIA, NDC 33342-128-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1005-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed content uniformity specifications for blend uniformity.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets 80 mg/25 mg, 30-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals Ltd. Baddi Himachal Pradesh, INDIA, NDC 33342-130-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0991-2019·2019-03-20

    Boehringer Ingelheim Recalls Mirapex Tablets Due to Low Weight

    Boehringer Ingelheim is recalling 112 cartons of Mirapex 1 mg tablets because routine stability testing identified low-weight tablets.

    Product
    Mirapex (pramipexole dihydrochloride) Tablets, 1 mg, 100-count unit-dose tablets per folding carton, Rx only, Distributed by: Boehringer Ingelheim (BI) Pharmaceuticals, Inc., Ridgefield, CT 06877 USA, Made in Germany, NDC 0597-0190-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0989-2019·2019-03-13

    Sunstone Organics Recalls Maeng Da Kratom Capsules Due to Salmonella Contamination

    Sunstone Organics is recalling Maeng Da Kratom capsules in 20, 60, and 150-count bottles because samples tested positive for Salmonella.

    Product
    Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 150 count capsules (UPC 00859667007163) , Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0986-2019·2019-03-13

    Sunstone Organics Recalls Maeng Da Kratom Powder Due to Salmonella Contamination

    Sunstone Organics is recalling Maeng Da Kratom powder in 25, 50, and 100-gram packages due to positive Salmonella test results.

    Product
    Maeng Da Kratom, packaged in a) 25 gram powder (UPC 00859667007118), b) 50 gram powder (UPC 00859667007125), c) 100 gram powder (UPC 00859667007132), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0518-2019·2019-03-13

    Leiter's Recalls Cefuroxime Intravitreal Injection Due to Incorrect Formulation

    Leiter's Enterprises is recalling 569 vials of Cefuroxime 10 mg/mL intravitreal injection because the drug was compounded with sterile water instead of sterile 0.9% Sodium Chloride.

    Product
    Cefuroxime 10 mg/mL in Sodium Chloride, Intravitreal injection, 1 mL in a 2mL Vial, Ophthalmic Use Only, Office Use Only, Leiter's (800) 292-6772- 17 Great Oaks Blvd., San Jose, CA 95119. NDC: 70360-007-35.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0520-2019·2019-03-13

    Vi-Jon Hydrogen Peroxide Recalled for IPA Contamination

    Vi-Jon, Inc. is recalling 32-ounce bottles of Hydrogen Peroxide First Aid Antiseptic due to the presence of Isopropyl Alcohol (IPA). The product was distributed in Ohio.

    Product
    Topical Solution USP Hydrogen Peroxide First Aid Antiseptic Oral Debriding Agent 32 Fl. Oz. (1 QT) 946 mL bottle, Distributed By: Discount Drug Mart 211 Commerce Drive, Medina, Ohio 44256 NDC 53943-871-45 UPC 0-93351-12758-8
    Category
    Drug
    Distribution
    1 state