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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2951–2975 of 8589

  • SevereFDA (Drugs)·D-0725-2019·2019-03-20

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

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

    Product
    Dr. King's SafeCare Rx Aversion to Change Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955280026, NDC 57955-2800-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0768-2019·2019-03-20

    King Bio Recalls ParaClenz Due to Microbial Contamination

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

    Product
    Dr. King's SafeCare Rx ParaClenz, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955001621, NDC 57955-0193-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0821-2019·2019-03-20

    FDA Recalls King Bio SafeCare Rx Obsessions/Compulsions Due to Microbial Contamination

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

    Product
    Dr. King's SafeCare Rx Obsessions/Compulsions, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955183020, NDC 57955-1831-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0877-2019·2019-03-20

    FDA Recalls Dr. King's SafeCare Rx Hangover Relief Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Hangover Relief bottles in the U.S., Canada, and Australia due to microbial contamination.

    Product
    Dr. King's SafeCare Rx Hangover Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955011323, NDC 57955-0113-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0878-2019·2019-03-20

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

    King Bio Inc. is recalling 130 bottles of Dr. King's SafeCare Rx Appetite Enhancer due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Appetite Enhancer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955012825, NDC 57955-0128-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0734-2019·2019-03-20

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

    King Bio Inc. is recalling specific lots of Dr. King's SafeCare Rx TUBR Miasm due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx TUBR Miasm, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955030423, NDC 57955-0304-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0647-2019·2019-03-20

    King Bio Recalls Homeopathic Caffeine Detox Due to Microbial Contamination

    King Bio Inc. is recalling 19 bottles of Dr. King's Natural Medicine Homeopathic Caffeine Detox due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Caffeine Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955540229, NDC 57955-6202-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0538-2019·2019-03-20

    King Bio Homeopathic Skin Irritations Recalled for Microbial Contamination

    King Bio Inc. is recalling 2,177 bottles of Dr. King's Natural Medicine Homeopathic Skin Irritations & Itch Relief due to microbial contamination.

    Product
    Dr. King's Natural Medicine Homeopathic Skin Irritations & Itch Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955516828, NDC 57955-5168-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0850-2019·2019-03-20

    FDA Recalls King Bio Tinnitus Relief Due to Microbial Contamination

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

    Product
    Dr. King's SafeCare Rx Tinnitus Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955027522, NDC 57955-0275-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0627-2019·2019-03-20

    King Bio Recalls Homeopathic Anti-Aging Product Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Anti-Aging & Wrinkles for Men due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Anti-Aging & Wrinkles for Men, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955814726, NDC 57955-8147-2
    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-0810-2019·2019-03-20

    FDA Recalls Dr. King's SafeCare Rx Leg Cramps & Spasms for Microbial Contamination

    King Bio Inc. is recalling 296 bottles of Dr. King's SafeCare Rx Leg Cramps & Spasms due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Leg Cramps & Spasms, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955043522, NDC 57955-0435-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0743-2019·2019-03-20

    King Bio Recalls Breast Cyst Discomfort Remedy Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Breast Cyst & Discomforts because the product may be contaminated with microorganisms.

    Product
    Dr. King's SafeCare Rx Breast Cyst & Discomforts, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000327, NDC 57955-0003-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0832-2019·2019-03-20

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

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

    Product
    Dr. King's SafeCare Rx Allergies: Food Chemicals U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955004226, NDC 57955-0042-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0766-2019·2019-03-20

    King Bio Recalls Dr. King's SafeCare Rx Allergies: Mold for Microbial Contamination

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

    Product
    Dr. King's SafeCare Rx Allergies: Mold, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955650126, NDC 57955-6501-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0913-2019·2019-03-20

    King Bio Recalls NET Remedies #11 Homeopathic Preparation Due to Microbial Contamination

    King Bio Inc. is recalling NET Remedies #11 Homeopathic Preparation, Oral Liquid, due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    NET Remedies #11 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-0975-2019·2019-03-20

    King Bio Recalls Homeopathic Formula Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Hyperactive High Potency Homeopathic Formula due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Hyperactive High Potency Homeopathic Formula, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955151029, NDC 57955-1511-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0640-2019·2019-03-20

    King Bio Recalls Homeopathic Ileocecal Valve Detox Due to Microbial Contamination

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

    Product
    Dr. King's Natural Medicine Homeopathic Ileocecal Valve Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955509820, NDC 57955-6083-2
    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-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
  • SevereFDA (Drugs)·D-0509-2019·2019-02-27

    ICU Medical Recalls 0.9% Sodium Chloride Injection Due to CGMP Deviations

    ICU Medical Inc. is voluntarily recalling 475,320 bags of 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0502-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 50 mg, because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 50 mg, a) 30-count bottle (NDC: 13668-409-30), b) 90-count bottle (NDC: 13668-409-90), c) 1000-count bottle (NDC: 13668-409-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0504-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because FDA labs found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP, 100 mg/12.5 mg, a) 90-count bottle (NDC: 13668-117-90), b) 1000-count bottle (NDC: 13668-117-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0503-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets because FDA testing found the impurity NDEA above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 25 mg, 90-count bottle (NDC: 13668-113-90), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide