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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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

8576–8600 of 17772

  • SevereFDA (Drugs)·D-0977-2019·2019-03-20

    King Bio Recalls Dr. King's Bronchial Care Due to Microbial Contamination

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

    Product
    Dr. King's Bronchial Care, 59 mL (liquid/liquid), Manufactured by: King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 Imported by Ambiental Solutions, Inc. Vancouver, BC, V5Y 1E6, DIN-HM 80035774 UPC 357955180425
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0696-2019·2019-03-20

    King Bio Recalls Cooling Acute Pain Relief Cream Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Cooling Acute Pain Relief Pure Homeopathic Cream due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Cooling Acute Pain Relief Pure Homeopathic Cream, 3 oz. (85 g), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955400134, NDC 57955-4001-3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0544-2019·2019-03-20

    King Bio Recalls Homeopathic Scar Freee Due to Microbial Contamination

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

    Product
    Dr. King's Natural Medicine Homeopathic Scar Freee, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955508724, NDC 57955-5087-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0934-2019·2019-03-20

    King Bio Recalls NET Remedies #3 Homeopathic Liquid Due to Microbial Contamination

    King Bio Inc. is recalling NET Remedies #3 Homeopathic Preparation due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    NET Remedies #3 (Blue Label) 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-0940-2019·2019-03-20

    King Bio Recalls NET Remedies #9 Homeopathic Preparation for Microbial Contamination

    King Bio Inc. is recalling NET Remedies #9 Homeopathic Preparation due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    NET Remedies #9 (Fuschia Label) 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-0679-2019·2019-03-20

    King Bio Recalls Homeopathic Flu Medicine Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Influenza Multi-Strain Flu Medicine due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Influenza Multi-Strain Flu Medicine Immune High Potency Homeopathic Formula for Professional Use Only, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955019923, NDC 57955-0298-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0758-2019·2019-03-20

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

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

    Product
    Dr. King's SafeCare Rx Chagrined, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955204022, NDC 57955-2041-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1059-2019·2019-03-20

    Mylan Recalls Levoleucovorin Injection Vials Due to Copper Salt Particulate Matter

    Mylan Institutional Inc is recalling specific lots of Levoleucovorin Injection due to the presence of copper salt particulate matter.

    Product
    Levoleucovorin Injection, 250 mg/25 mL, (10 mg/mL), 25 mL Single-Use Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 U.S.A., Made in India. NDC: 67457-601-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0638-2019·2019-03-20

    King Bio Homeopathic Fears & Nightmares Recalled for Microbial Contamination

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

    Product
    Dr. King's Natural Medicine Homeopathic Fears & Nightmares, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955509929, NDC 57955-5099-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0929-2019·2019-03-20

    King Bio Recalls NET Remedies #12 Homeopathic Liquid Due to Microbial Contamination

    King Bio Inc. is recalling NET Remedies #12 Homeopathic Preparation due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    NET Remedies #12 (Pink Label) 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-0783-2019·2019-03-20

    King Bio Recalls Aller-Detox Product Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Aller-Detox: Food Additives & Preservatives due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Aller-Detox: Food Addititives & Preservatives, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955240525, NDC 57955-2405-2
    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
  • 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
  • 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-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
  • 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
  • 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-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-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
  • ModerateFDA (Drugs)·D-1066-2019·2019-03-13

    Ascend Recalls Tamsulosin Hydrochloride Capsules Due to Dissolution Failure

    Ascend Laboratories is recalling 3,072 bottles of Tamsulosin Hydrochloride 0.4 mg capsules because stability testing revealed high out-of-specification dissolution results.

    Product
    TAMSULOSIN HYDROCHLORIDE — TAMSULOSIN HYDROCHLORIDE (TAMSULOSIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide