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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6176–6200 of 11856

  • SevereFDA (Drugs)·D-0730-2018·2018-05-16

    Vitalab Pharmacy Recalls Sterile Injectable Drug Due to Sterility Concerns

    Vitalab Pharmacy is recalling 22 vials of a sterile injectable drug because airflow patterns may not support aseptic production, raising sterility concerns.

    Product
    Papaverine 9mg/Phentolamine 1mg/Atropine 0.1mg/Prostaglandinl 10mcg/ml, sterile injectable, Vitalab Pharmacy, Inc
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0735-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Albuterol Inhalation Solution Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Albuterol 0.083% Inhalation Solution due to a lack of processing controls. The affected lots were dispensed in five states between December 2017 and February 2018.

    Product
    Albuterol 0.083% Inh Sol. 30 days supply, Rx Only, 39183, NDC 76204-0200-60, 30
    Category
    Drug
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0792-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Bendeka Due to Lack of Processing Controls

    Kroger Specialty Pharmacy is recalling Bendeka 25 mg/mL 4 mL MDVPF due to a lack of processing controls. The affected product was dispensed in five states between December 2017 and February 2018.

    Product
    Bendeka 25 mg/mL 4 mL MDVPF NDC 63459-0348-04 28 days supply
    Category
    Drug
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0728-2018·2018-05-16

    Vitalab Methylcobalamin Injection Recalled Due to Sterility Concerns

    Vitalab Pharmacy is recalling 178 vials of Methylcobalamin for injection because airflow patterns may not support aseptic production, raising sterility concerns.

    Product
    Methylcobalamin for injection, 1mg/mL and 10 mg/mL, Sterile injectable, Vitalab Pharmacy, Inc
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0797-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Tasigna Capsules Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Tasigna Capsules 150 mg due to a lack of processing controls. The affected units were dispensed in five states between December 2017 and February 2018.

    Product
    Tasigna Capsules 150 mg NDC 00078-0592-87 28 days supply
    Category
    Drug
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0754-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Azithromycin Tablets Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Azithromycin 250 mg tablets due to a lack of processing controls. The affected lots were dispensed in five states between December 2017 and February 2018.

    Product
    Azithromycin 250 mg tablet #18 TEV NDC 50111-0787-66 28 days supply
    Category
    Drug
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0791-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Capecitabine Tablets Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Capecitabine 500 mg tablets due to a lack of processing controls. The affected lots were dispensed in five states between December 2017 and February 2018.

    Product
    Capecitabine 500 mg Tablet NDC 00378-2512-78 28 days supply and 21 days supply
    Category
    Drug
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0866-2018·2018-05-16

    AuroMedics Recalls Ampicillin and Sulbactam Injection Due to Particulate Matter

    AuroMedics Pharma LLC is recalling 54,720 vials of Ampicillin and Sulbactam for Injection due to confirmed reports of visible red rubber particles.

    Product
    AMPICILLIN AND SULBACTAM — AMPICILLIN AND SULBACTAM (AMPICILLIN SODIUM AND SULBACTAM SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0732-2018·2018-05-16

    Vitalab Pharmacy Recalls Sterile Injectable Drugs Due to Sterility Concerns

    Vitalab Pharmacy is recalling specific lots of sterile injectable drugs because airflow patterns may not support aseptic production, raising sterility concerns.

    Product
    Papaverine 30mg/Phentolamine 1.5mg/Prostaglandin 50mcg/mL, sterile injectable, ST3:Papaverine 40mg/Phentolamine 3mg/Prostaglandin 60mcg/mL, Vitalab Pharmacy, Inc.
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Drugs)·D-0733-2018·2018-05-16

    Vitalab Pharmacy Recalls Sterile Injectable Drugs Due to Sterility Concerns

    Vitalab Pharmacy is recalling specific lots of sterile injectable drugs because airflow patterns may not support aseptic production.

    Product
    Papaverine 30mg/Phentolamine 2mg/Prostaglandin 20mcg/mL, Papaverine 30mg/Phentolamine 1mg/Prostaglandin 10mcg/mL, Papaverine 30mg/Phentolamine 1mg/Prostaglandin 25mcg/mL, sterile injectables, Vitalab Pharmacy, Inc
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Drugs)·D-0773-2018·2018-05-16

    Kroger Recalls Revlimid Due to Lack of Processing Controls

    Kroger Specialty Pharmacy is recalling Revlimid 20 mg oral capsules because of a lack of processing controls. The recall affects specific lots distributed in MS, LA, AR, IL, and FL.

    Product
    Revlimid 20 mg oral cap NDC 59572-0420-21 28 days supply
    Category
    Drug
    Distribution
    5 states
  • HighFDA (Drugs)·D-0776-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Avonex PFS Kits Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Avonex 30 mcg/0.5 mL PFS Kits due to a lack of processing controls. The affected units were dispensed in five states between December 2017 and February 2018.

    Product
    Avonex 30 mcg/0.5 mL PFS Kit NDC 59627-0222-05 28 days supply
    Category
    Drug
    Distribution
    5 states
  • HighFDA (Drugs)·D-0790-2018·2018-05-16

    Kroger Recalls Capecitabine Tablets Due to Lack of Processing Controls

    Kroger Specialty Pharmacy is recalling one lot of Capecitabine 150 mg tablets because the product lacks required processing controls. The recall affects units dispensed in Mississippi, Louisiana, Arkansas, Illinois, and Florida.

    Product
    Capecitabine 150 mg Tablet NDC 00378-2511-91 28 days supply
    Category
    Drug
    Distribution
    5 states
  • HighFDA (Drugs)·D-0739-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Pulmicort Respules Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Pulmicort Respules 0.5 mg/2mL due to a lack of processing controls. The affected units were dispensed in five states between December 2017 and February 2018.

    Product
    Pulmicort Respules 0.5 mg/2mL s, 30 days supply, NDC 00186-1989-04
    Category
    Drug
    Distribution
    5 states
  • HighFDA (Drugs)·D-0784-2018·2018-05-16

    Kroger Recalls Sprycel Tablets Due to Lack of Processing Controls

    Kroger Specialty Pharmacy is recalling Sprycel 100 mg tablets because of a lack of processing controls. The affected product was distributed in Mississippi, Louisiana, Arkansas, Illinois, and Florida.

    Product
    Sprycel 100 mg tablet NDC 00003-0852-22 30 days supply
    Category
    Drug
    Distribution
    5 states
  • HighFDA (Drugs)·D-0800-2018·2018-05-16

    Kroger Recalls Lupron Depot Due to Lack of Processing Controls

    Kroger Specialty Pharmacy is recalling Lupron Depot 22.5 mg 3 month Kits due to a lack of processing controls. The recall affects lots dispensed in MS, LA, AR, IL, and FL between December 2017 and February 2018.

    Product
    Lupron Depot 22.5 mg 3 month Kit NDC 00074-3346-03 84 days supply
    Category
    Drug
    Distribution
    5 states
  • HighFDA (Drugs)·D-0747-2018·2018-05-16

    Kroger Recalls Botox Due to Lack of Processing Controls

    Kroger Specialty Pharmacy is recalling Botox 100 Units Vials because of a lack of processing controls. The product was distributed in MS, LA, AR, IL, and FL.

    Product
    Botox 100 Units Vial NDC 00023-1145-01 90 days supply.
    Category
    Drug
    Distribution
    5 states