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 categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

3826–3850 of 18005

  • ModerateFDA (Drugs)·D-1127-2022·2022-06-22

    Homeopathic Drug Recall: Candida Albicans Remedy for Manufacturing Quality Issues

    Washington Homeopathic Products is recalling Candida Albicans homeopathic remedy due to manufacturing quality control violations. The voluntary recall affects 1,047 bottles distributed nationwide.

    Product
    Candida Albicans, Potency: 9C, 10C, 12C, 13C, 14C 15C 16C, 19C, 24C, 25C, 26C, 30C, 200C, 14X, 15X, 16X, 20X, 288X, 30X, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22160·2022-06-16

    Kroger Aspirin and Ibuprofen Recalled for Lack of Child-Resistant Packaging

    Time-Cap Labs is recalling Kroger-brand aspirin and ibuprofen products because the bottles lack child-resistant packaging required by law, posing a poisoning risk to young children who may swallow the contents.

    Product
    Kroger Aspirin, 300 count bottles and Ibuprofen, 160 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22162·2022-06-16

    Kroger Acetaminophen Recalled for Non-Child-Resistant Packaging

    Sun Pharmaceutical is recalling Kroger brand acetaminophen 650 mg extended-release caplets because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act, posing a risk of poisoning if swallowed by young children.

    Product
    Kroger Acetaminophen, 100 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22161·2022-06-16

    Walgreens Acetaminophen Bottles Recalled for Non-Compliant Packaging

    Aurohealth recalled Walgreens brand acetaminophen 500 mg bottles (150 count) because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act, posing a poisoning risk to young children.

    Product
    Walgreens Pain Reliever Acetaminophen, 150 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22164·2022-06-16

    Kroger Arthritis Pain Acetaminophen Recalled for Non-Child-Resistant Packaging

    Kroger-brand acetaminophen tablets in 225-count bottles lack required child-resistant packaging, posing a poisoning risk to young children if ingested. About 25,660 units were sold nationwide from December 2021 through March 2022.

    Product
    Kroger Arthritis Pain Acetaminophen, 225 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1167-2022·2022-06-15

    Tacrolimus Compounded Suspension Recalled Due to Subpotency

    Valor Compounding Pharmacy recalls compounded Tacrolimus 0.5 mg/mL suspension due to subpotency. The medication, distributed in California, may not provide adequate therapeutic levels for immunosuppression in transplant patients.

    Product
    Tacrolimus (Brand Capsules ) 0.5 mg/mL Suspension, Rx, This is a compounded medication., Valor Compounding Pharmacy, 2461 Shattuck Ave., Berkeley, CA 94704,
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1168-2022·2022-06-15

    FDA Recalls Compounded Tacrolimus Suspension Due to Subpotency

    Valor Compounding Pharmacy issued a Class I recall for compounded Tacrolimus suspension (Lot 04272022@35) distributed in California due to subpotency.

    Product
    Tacrolimus (Brand Capsules ) 0.5 mg/mL Suspension, Rx, This is a compounded medication., Valor Compounding Pharmacy, 2461 Shattuck Ave., Berkeley, CA 94704
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-1013-2022·2022-06-15

    FDA Recalls Epinephrine Auto-Injectors Due to Temperature Abuse

    McKesson is recalling 55 packs of epinephrine auto-injectors nationwide due to temperature abuse during manufacturing. This represents a deviation from manufacturing standards.

    Product
    EPINEPHRINE — EPINEPHRINE (EPINEPHRINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1088-2022·2022-06-15

    Levofloxacin 500 mg Tablets Recalled Due to Manufacturing Temperature Abuse

    Mckesson Medical-Surgical is recalling Levofloxacin 500 mg tablets nationwide due to temperature abuse during manufacturing that violated pharmaceutical quality standards.

    Product
    LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1060-2022·2022-06-15

    FDA Recalls Medroxyprogesterone Acetate Injectable Suspension for Temperature Abuse

    McKesson Medical-Surgical recalls 780 vials of medroxyprogesterone acetate injectable suspension nationwide due to temperature exposure during distribution that may affect medication stability.

    Product
    Medroxyprogesterone acetate injectable suspension, 150 mg/mL, 1 mL single dose vial, Rx only, MFG: NorthStarRx/Teva Pharma USA , NDC 16714-981-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1076-2022·2022-06-15

    FDA Recalls Proair HFA Albuterol Inhalation Aerosol for Temperature Abuse

    The FDA recalled 56 units of Proair HFA (albuterol sulfate) inhalation aerosol due to temperature abuse during manufacturing. The affected products were distributed nationwide.

    Product
    Proair, HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation, 200 metered inhalations, Rx only, MFG: Teva Pharma USA, NDC 59310-579-22
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0987-2022·2022-06-15

    B-Complex plus Chromic Chloride injection recall for lack of sterility assurance

    US Specialty Formulations is recalling B-Complex plus Chromic Chloride injectable vials due to lack of assurance of sterility. The product was distributed to medical facilities and physician offices nationwide.

    Product
    B-Complex + Chromic Chloride (Choline Chloride 3%, Inositol 3%, Pyridoxine HCl 2%, Niacinamide 2%, Thiamine HCl 2%, Chlorobutanol 0.5%, Riboflavin 0.05%, Chromic Chloride 0.003%), 30 mL Multi-Dose Vial, packaged in 2 x 30 mL Multi-Dose Vials per carton, US Specialty Formulations
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1007-2022·2022-06-15

    FDA Issues Class II Recall of Sumatriptan Injection Due to Temperature Exposure

    McKesson Medical-Surgical is recalling Sumatriptan Injection, USP, 6mg/0.5mL nationwide due to temperature abuse during distribution that may have affected medication stability and potency.

    Product
    Sumatriptan Injection, USP, 6mg/0.5 mL, packaged in a box of 5 x 0.5 mL single-dose vials, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0173-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1015-2022·2022-06-15

    Firmagon Injection Recalled Due to Manufacturing Temperature Abuse

    McKesson Medical-Surgical is recalling 25 kits of Firmagon (degarelix for injection) 80 mg nationwide due to temperature abuse during manufacturing. No illnesses have been reported.

    Product
    Firmagon (degarelix for injection) 80 mg, Maintenance Dose (28 days), packaged in a kit, Rx only, MFG: Ferring Pharmaceuticals Inc., NDC 55566-8303-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1046-2022·2022-06-15

    Hydroxyzine Pamoate Capsules Recalled Due to Temperature Abuse During Manufacturing

    McKesson Medical-Surgical is recalling Hydroxyzine Pamoate Capsules due to cGMP deviations from temperature abuse during manufacturing, which may affect drug stability and potency.

    Product
    HYDROXYZINE PAMOATE — HYDROXYZINE PAMOATE (HYDROXYZINE PAMOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1115-2022·2022-06-15

    Prescription anesthetic Diprivan recalled for manufacturing temperature deviation

    McKesson is recalling Diprivan (Propofol) injection due to manufacturing temperature deviations that may affect drug stability. The FDA Class II recall involves 122 cartons distributed nationwide to medical settings.

    Product
    DIPRIVAN — DIPRIVAN (PROPOFOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1079-2022·2022-06-15

    Vecuronium Bromide for Injection Recalled for Manufacturing Temperature Deviation

    McKesson Medical-Surgical is recalling Vecuronium Bromide for Injection (10 mg) manufactured by Teva Pharma USA due to cGMP deviations involving temperature abuse during production. The product was distributed nationwide; no illnesses have been reported.

    Product
    Vecuronium Bromide for Injection, 10 mg (1mg/ mL) vial, 10-count box, Rx only, MFG: Teva Pharma USA, NDC 0703-2914-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1100-2022·2022-06-15

    Verapamil HCL injection recalled due to temperature abuse during manufacturing

    McKesson Medical-Surgical is recalling Verapamil HCL injection ampules (NDC 04094-011-01) distributed nationwide due to temperature abuse during manufacturing.

    Product
    Verapamil HCL, ampule, 2.5 mg/ML 2ML (5/pack), Rx only, MFG: Pfizer, NDC 04094-011-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1064-2022·2022-06-15

    MethylPREDNISolone Acetate Injectable Suspension Recalled Due to Temperature Exposure

    McKesson Medical-Surgical is recalling MethylPREDNISolone Acetate Injectable Suspension due to temperature abuse during distribution. The drug was exposed to conditions that could affect its quality and safety.

    Product
    MethyLPREDNISolone Acetate Injectable Suspension USP, 400 mg/5 mL (80 mg/mL), 5 mL Multiple Dose Vial, Rx only, MFG: NorthstarRx/Teva Pharma USA, NDC 16714-473-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1094-2022·2022-06-15

    Labetalol Hydrochloride Tablets Recalled for Temperature Abuse During Manufacturing

    McKesson Medical-Surgical is recalling Labetalol Hydrochloride Tablets 100 mg due to temperature abuse during manufacturing that may affect drug stability. This Class II recall affects units distributed nationwide.

    Product
    Labetalol Hydrochloride Tablets, USP, 100 mg, 100-count bottle, Rx only, MFG: Par Pharma, NDC 49884-122-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1029-2022·2022-06-15

    Ciprofloxacin eye drops recalled due to manufacturing temperature deviations

    McKesson is recalling Ciprofloxacin Ophthalmic Solution 0.3% nationwide due to temperature deviations during manufacturing. The FDA classifies this as a Class II recall.

    Product
    Ciprofloxacin Ophthalmic Solution 0.3%, 10 mL bottle, Rx only, Manufactured by: Alcon Laboratories, Inc., NDC 61314-0656-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1089-2022·2022-06-15

    Injectable Steroid Suspension Recalled Due to Manufacturing Temperature Control Deviation

    Celestone Soluspan injectable suspension is being recalled for manufacturing temperature control deviations that violated good manufacturing practices. McKesson distributed 51 vials nationwide.

    Product
    Celestone Soluspan (betamethasone sodium phosphate and betametasone acetate injectable suspension 6 mg/mL, 30 mg/5mL, multidose vial, Rx only, MFG: Merck Company, NDC 0085-4320-01
    Category
    Drug
    Distribution
    Distributed nationwide