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 the agency’s own highest classification or reported deaths or serious injuries, 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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12026–12050 of 36637

  • SevereFDA (Drugs)·D-0660-2020·2020-01-22

    Sun Pharma Recalls Sumatriptan Tablets Due to Impurity Failures

    Sun Pharmaceutical Industries is recalling 207,585 blisters of Sumatriptan Succinate 100 mg tablets due to failed impurity specifications.

    Product
    Sumatriptan Succinate Tablets, 100 mg packaged in 9 (1X9) Unit-of-use blister card, (62756-0522-69), Rx only, Sun Pharma, Cranbury, NJ
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0682-2020·2020-01-22

    Assurance Infusion Recalls BUP 10MG/HYDROM 15MG/SUF 200MCG/ML Injection Syringes

    Assurance Infusion is recalling specific lots of BUP 10MG/HYDROM 15MG/SUF 200MCG/ML Injection syringes due to a lack of sterility assurance.

    Product
    BUP 10MG/HYDROM 15MG/SUF 200MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0681-2020·2020-01-22

    Assurance Infusion Recalls Multi-Drug Injection Due to Sterility Concerns

    Assurance Infusion is recalling a specific lot of multi-drug injection syringes due to a lack of sterility assurance. The product was distributed nationwide.

    Product
    BUP 10MG/HYDROM 10MG/MORP 2MG/SUF 250MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0743-2020·2020-01-22

    Assurance Infusion Recalls Hydromorphone Syringes Due to Sterility Concerns

    Assurance Infusion is recalling specific lots of Hydromorphone 2mg/mL injection syringes because of a lack of sterility assurance.

    Product
    HYDROMORPHONE 2MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0679-2020·2020-01-22

    Assurance Infusion Recalls BPC-157 Vials Due to Sterility Concerns

    Assurance Infusion is recalling BPC-157 vials nationwide because the product lacks sterility assurance.

    Product
    BPC-157 2000 mcg/mL in 5 mL vials Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0817-2020·2020-01-22

    Physio-Control Recalls LIFEPAK 15 Monitor/Defibrillator Service Kits

    Physio-Control is recalling 705 LIFEPAK 15 Monitor/Defibrillator service kits because oxidation may prevent the device from delivering a shock.

    Product
    LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0739-2020·2020-01-22

    Assurance Infusion Recalls Hydrom Injection Due to Sterility Concerns

    Assurance Infusion is recalling Hydrom 1mg/Morp 20mg/Suf 100mcg/mL injection syringes due to a lack of sterility assurance.

    Product
    HYDROM 1MG/MORP 20MG/SUF 100MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0716-2020·2020-01-22

    Assurance Infusion Recalls BUP 675MCG/MORP 20MG/ML Injection Syringes

    Assurance Infusion is recalling BUP 675MCG/MORP 20MG/ML Injection syringes due to a lack of sterility assurance.

    Product
    BUP 675MCG/MORP 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0672-2020·2020-01-22

    Assurance Infusion Recalls Baclofen and Fentanyl Injection Due to Sterility Concerns

    Assurance Infusion is recalling specific lots of Baclofen and Fentanyl Injection due to a lack of sterility assurance. The product was distributed nationwide.

    Product
    BAC 4000MCG /FENT 600MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0509-2020·2020-01-22

    Veggie Noodle Co Recalls Fresh Veggie Ramen for Listeria Risk

    Veggie Noodle Co is recalling Cece's Veggie Co. brand Fresh Veggie Ramen with Chicken Broth due to potential contamination with Listeria monocytogenes.

    Product
    Cece's Veggie Co. brand Fresh Veggie Ramen with Chicken Broth (11.5 oz, UPC 5228700653) packaged in a plastic tray
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0671-2020·2020-01-22

    Assurance Infusion Recalls BAC/FENT/MORP Injection Due to Sterility Concerns

    Assurance Infusion is recalling a specific lot of BAC/FENT/MORP injection due to a lack of sterility assurance. The product was distributed nationwide.

    Product
    BAC 250MCG/ /FENT 3500MCG/ /MORP 25MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0696-2020·2020-01-22

    Assurance Infusion Recalls BUP 23MG/HYDROM 25MG/SUF 100MCG/ML Injection Syringes

    Assurance Infusion is recalling BUP 23MG/HYDROM 25MG/SUF 100MCG/ML Injection syringes due to a lack of sterility assurance. The recall covers nationwide distribution.

    Product
    BUP 23MG/HYDROM 25MG/SUF 100MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0750-2020·2020-01-22

    Assurance Infusion Recalls Morphine Sulfate Injection Due to Sterility Concerns

    Assurance Infusion is recalling Morphine Sulfate Injection in 20 mL syringes due to a lack of sterility assurance. The product was distributed nationwide.

    Product
    MORP 20MG/SUF 70MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0734-2020·2020-01-22

    Assurance Infusion Recalls HCG Injection Vials Due to Sterility Concerns

    Assurance Infusion is recalling HCG 1,000U/1ML injection vials nationwide due to a lack of sterility assurance. Consumers should stop using the product and contact their healthcare provider.

    Product
    HCG 1,000U/1ML INJ in 4 mL vial Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0714-2020·2020-01-22

    Assurance Infusion Recalls BUP 5MG/MORP 10MG/ML Injection Due to Sterility Concerns

    Assurance Infusion is recalling BUP 5MG/MORP 10MG/ML Injection in 20 mL syringes due to a lack of sterility assurance. The recall covers lots distributed nationwide.

    Product
    BUP 5MG/MORP 10MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide