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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9651–9675 of 17987

  • ModerateFDA (Drugs)·D-0777-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Ibrance Capsules Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Ibrance 125 mg capsules due to a lack of processing controls. The recall covers units dispensed in five states between December 2017 and February 2018.

    Product
    Ibrance 125 mg cap NDC 00069-0189-21 28 days supply
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0734-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Humira Pen Kits Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Humira Pen Sub-q and Psor Kits due to a lack of processing controls. The affected products were dispensed in five states between December 2017 and February 2018.

    Product
    Humira Pen Sub-q Kit a.) 40 mg/0.8 mL (NDC 00074-4339-02); Humira Pen Psor Kit b.) 40 mg/0.8 mL (NDC 00074-4339-07) 28 day supply, Rx Only,
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0775-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Revlimid Capsules Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Revlimid 25 mg oral capsules due to a lack of processing controls. The affected lots were dispensed between December 2017 and February 2018.

    Product
    Revlimid 25 mg oral cap NDC 59572-0425-21 28 days supply
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0862-2018·2018-05-16

    Noven Recalls Minivelle Estradiol Patches Due to Adhesive Defect

    Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal systems because the adhesive may not meet specifications, causing patches to stick poorly to the skin.

    Product
    MINIVELLE — MINIVELLE (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0764-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Praluent 75 mg Pens for Processing Control Issues

    Kroger Specialty Pharmacy is recalling Praluent 75 mg pens due to a lack of processing controls. The affected units were dispensed in five states between December 2017 and February 2018.

    Product
    Praluent 75 mg Pen (2 pens/Pkg) NDC 00024-5901-02 28 days supply
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0755-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Creon DR Capsules Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Creon DR 24,000 Units capsules due to a lack of processing controls. The affected products were dispensed in five states.

    Product
    Creon DR 24,000 Units Capsule #250 NDC 00032-1224-07 30 days supply
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0788-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Sutent 50 mg Capsules Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Sutent 50 mg capsules due to a lack of processing controls. The affected products were dispensed in five states between December 2017 and February 2018.

    Product
    Sutent 50 mg capsules x28 NDC 00069-0550-38 42 days supply
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0746-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Enbrel PFS Due to Processing Control Issues

    Kroger Specialty Pharmacy is recalling Enbrel PFS 50 mg/mL injections due to a lack of processing controls. The affected lots were dispensed between December 2017 and February 2018.

    Product
    Enbrel PFS 50 mg/mL Inj #4 NDC 58406-0435-04 28 days supply;
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0787-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Sutent 37.5 mg Capsules Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Sutent 37.5 mg capsules due to a lack of processing controls. The affected products were dispensed in five states between December 2017 and February 2018.

    Product
    Sutent 37.5 mg capsules x28 NDC 00069-0830-38 28 days supply
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0760-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Dupixent Due to Processing Control Issues

    Kroger Specialty Pharmacy is recalling Dupixent 300 mg/2 mL prefilled syringes due to a lack of processing controls. The recall affects units dispensed in five states between December 2017 and February 2018.

    Product
    Dupixent 300 mg/2 mL PFS #2 w/ NS NDC 00024-5914-01 28 days supply
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0781-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Temozolomide Due to Processing Control Issues

    Kroger Specialty Pharmacy is recalling Temozolomide 250 mg capsules due to a lack of processing controls. The recall affects specific lots dispensed between December 2017 and February 2018.

    Product
    Temozolomide 250 mg NDC 43975-0257-05 28 days supply
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0749-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Kitabis Pak Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Kitabis Pak 300 mg/5 mL Soln due to a lack of processing controls. The product was distributed in five states.

    Product
    Kitabis Pak 300 mg/5 mL Soln PARI #56 NDC 24492-0850-56 56 days supply
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0774-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Revlimid Capsules Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Revlimid 5 mg oral capsules due to a lack of processing controls. The affected lots were dispensed in five states between December 2017 and February 2018.

    Product
    Revlimid 5 mg oral cap NDC 59572-0405-28 28 days supply
    Category
    Drug
    Distribution
    5 states
  • LowFDA (Drugs)·D-0828-2018·2018-05-16

    Septodont Recalls OraVerse Injection Due to Impurity Test Failure

    Septodont Inc. is recalling OraVerse (Phentolamine Mesylate) Injection due to an out-of-specification result for a degradation product impurity.

    Product
    ORAVERSE — ORAVERSE (PHENTOLAMINE MESYLATE)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0804-2018·2018-05-09

    Sanofi Recalls Over-Concentrated Docetaxel Injection Vials Nationwide

    Sanofi-Aventis is recalling 19,580 vials of Docetaxel injection concentrate due to potential over-concentration. The affected lots were distributed nationwide.

    Product
    DOCETAXEL — DOCETAXEL (DOCETAXEL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0708-2018·2018-05-09

    AuroMedics Recalls Levofloxacin Injection Bags Due to Sterility Concerns

    AuroMedics Pharma LLC is recalling specific lots of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and reports of leaking bags with mold.

    Product
    LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN IN 5% DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0705-2018·2018-05-09

    AuroMedics Recalls Levetiracetam Injection Due to Sterility Concerns

    AuroMedics Pharma LLC is recalling 261,250 bags of Levetiracetam Injection due to a confirmed report of leaking bags and mold found between the outer bag and overwrap.

    Product
    LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM IN SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide