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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9201–9225 of 36630

  • SevereNHTSA·21E081000·2021-08-25

    Deking LP Regulators Recalled Due to Fire Risk from Excessive Pressure

    Deking Corporation is recalling Winntec and WIC Model 6020 LP regulators installed in recreational vehicles. The parts may fail and cause excessive gas pressure, increasing the risk of fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V661000·2021-08-25

    2022 Thomas Built Buses Minotour Recalled for Weak Side Panel Joints

    Daimler Trucks North America is recalling 2022 Thomas Built Buses Minotour school buses because adhesive may not have been properly applied, resulting in insufficient joint strength.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V658000·2021-08-25

    Summit Trailer Recalls One 2017 AD45 for Steering Arm Defect

    Summit Trailer Sales is recalling one 2017 AD45 trailer because the steering arm may detach, potentially causing loss of steering control or a road hazard.

    Product
    SUMMIT — SUMMIT AD45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E079000·2021-08-25

    Rigid Hitch Recalls Specific Tow Hitches Due to Weld Defects

    Rigid Hitch is recalling certain DHB-series tow hitches because incorrect welding settings may cause the weld to fail, increasing the risk of a crash.

    Product
    STRUCTURE:BODY:TAILGATE:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0873-2021·2021-08-25

    Bacon Ranch Seasoning Recalled for Salmonella Contamination

    Mane Inc is recalling Flavored Bacon Ranch Seasoning packaged in 25lb kraft paper bags due to Salmonella detected in an ingredient used during manufacturing. The affected product was distributed to manufacturers in Ohio, Indiana, Minnesota, and Oregon.

    Product
    Flavored Bacon Ranch Seasoning Packaged in 25lb kraft paper bags
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0874-2021·2021-08-25

    BBQ Seasoning Recalled Due to Salmonella Contamination

    Mane Inc is recalling BBQ seasoning products because an ingredient tested positive for Salmonella. The recall affects seasoning distributed to manufacturers in Ohio, Indiana, Minnesota, and Oregon.

    Product
    BBQ Seasoning Packaged in 50lb poly bag/cardboard box combo and kraft paper bags
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0921-2021·2021-08-25

    Lebenswert Anfangsmilch Stage 1 Infant Formula Recall for Inadequate Iron and Labeling

    Able Groupe Inc is recalling Lebenswert Anfangsmilch Stage 1 Organic Infant Milk Formula because some products contain insufficient iron and lack required FDA labeling. The formula may not provide adequate iron for certain infants, including premature infants and those with low birth weight.

    Product
    Lebenswert Anfangsmilch Stage 1 Organic Infant Milk Formula
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0735-2021·2021-08-25

    Teva Vecuronium Bromide Injection Recalled for Sterility Assurance

    Teva Pharmaceuticals USA is recalling Vecuronium Bromide for Injection 10 mg vials nationwide due to lack of assurance of sterility. The recall affects 62,358 vials distributed across multiple lots.

    Product
    Vecuronium Bromide for Injection 10 mg, 10mL vial, Rx only, Teva Pharmaceuticals USA, North Wales, PA 19454, NDC 0703-2914-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0911-2021·2021-08-25

    HiPP Dutch Stage 2 Infant Formula Missing Pre-Market Approval and Labeling

    Able Groupe Inc is recalling HiPP Dutch Stage 2 Combiotic Follow-on Milk Formula because required pre-market notifications were not submitted to the FDA and products lack mandatory English labeling statements.

    Product
    HiPP Dutch Stage 2 Combiotic Follow-on Milk Formula
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0739-2021·2021-08-25

    Teva Norepinephrine Bitartrate Injection Recalled for Sterility Assurance

    Teva Pharmaceuticals USA is recalling Norepinephrine Bitartrate Injection, USP 4 mg/4 mL vials due to lack of assurance of sterility. The product was distributed nationwide.

    Product
    Norepinephrine Bitartrate Injection, USP 4 mg/4 mL, 4 mL single dose vials, packaged in 10 vial cartons (NDC 0703-1153-03) Rx only, Teva Pharmaceuticals USA Inc. North Wales, PA 19454, vial NDC 0703-1153-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0741-2021·2021-08-25

    Metoclopramide Injection Vials Recalled for Lack of Sterility Assurance

    Teva Pharmaceuticals USA is recalling 25,653 vials of Metoclopramide Injection USP due to lack of assurance of sterility. The affected vials were distributed nationwide, including Puerto Rico.

    Product
    METOCLOPRAMIDE — METOCLOPRAMIDE (METOCLOPRAMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0916-2021·2021-08-25

    Holle Bio Stage 1 Organic Infant Formula Recall for Inadequate Iron Content and Labeling

    Able Groupe Inc is recalling Holle Bio Stage 1 Organic Infant Milk Formula because the product may contain insufficient iron for some infants and lacks required FDA labeling statements. The recall affects approximately 76,000 units sold directly through littlebundle.com.

    Product
    Holle Bio Stage 1 Organic Infant Milk Formula
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0914-2021·2021-08-25

    HiPP German Stage 1 Infant Formula Lacks FDA Pre-Market Notification

    Able Groupe Inc is recalling HiPP German Stage 1 Combiotic Infant Milk Formula because required FDA pre-market notifications were not submitted. Some units contain inadequate iron levels and lack required English labeling.

    Product
    HiPP German Stage 1 Combiotic Infant Milk Formula
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0733-2021·2021-08-25

    Amikacin Sulfate Injection Recalled Due to Sterility Assurance Failure

    Teva Pharmaceuticals USA is recalling Amikacin Sulfate Injection USP 1 gram/4mL vials nationwide due to lack of assurance of sterility. The recall affects 4,712 vials with lot #31329243B and expiration date 05/2022.

    Product
    Amikacin Sulfate Injection USP 1 gram/4mL (250mg/ML), 4 mL single-dose vials, Rx only, Teva Pharmaceuticals USA Inc. North Wales, PA 19454, NDC 0703-9040-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0907-2021·2021-08-25

    HiPP Comfort Milk Formula Recalled for Inadequate Iron and Labeling Violations

    Able Groupe Inc is recalling HiPP Comfort Milk Formula because some products contain insufficient iron and lack required labeling. The formula may not provide adequate iron for certain infants, particularly premature or low-birth-weight infants.

    Product
    HiPP Comfort Milk Formula
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0737-2021·2021-08-25

    Leucovorin Calcium Injection Recalled Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection (350 mg/vial) distributed nationwide because the manufacturer cannot assure the product meets sterility standards.

    Product
    Leucovorin Calcium for Injection, USP 350 mg/vial, 17.5 mL single-use vials, Rx only, Teva Parenteral Medicines, Inc. Irvine, CA 92618, NDC 0703-5145-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0742-2021·2021-08-25

    Teva Alprostadil Injection Recalled for Lack of Sterility Assurance

    Teva Pharmaceuticals USA is recalling one lot of Alprostadil Injection USP due to lack of assurance of sterility. The affected product was distributed nationwide, including Puerto Rico.

    Product
    Alprostadil Injection USP, 500 mg/mL, 1 mL single dose, vials, 5 mL single use vial per carton (NDC 0703-1501-02), Rx only, Teva Pharmaceuticals USA, Inc. Parsippany, NJ 07054, Vial NDC 0703-1501-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0910-2021·2021-08-25

    HiPP HA Infant Formula Recalled for Inadequate Iron and Missing Labeling

    Able Groupe Inc is recalling HiPP HA Germany Hypoallergenic Stage PRE Combiotic Infant Milk Formula (76,000 units) because some products contain less than the required iron per serving and lack mandatory FDA-compliant English labeling.

    Product
    HiPP HA Germany Hypoallergenic Stage PRE Combiotic Infant Milk Formula
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0922-2021·2021-08-25

    Lebenswert Stage 2 Infant Formula Recalled for Missing Labeling

    Able Groupe Inc is recalling Lebenswert Folgemilch Stage 2 Organic Follow-On Infant Milk Formula (76,000 units) sold directly through littlebundle.com. The formula was not submitted for required FDA pre-market notification and lacks mandatory English-language labeling.

    Product
    Lebenswert Folgemilch Stage 2 Organic Follow-On Infant Milk Formula
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0909-2021·2021-08-25

    HiPP Dutch Stage 1 Infant Formula Recalled for Inadequate Iron Content

    Able Groupe Inc is recalling HiPP Dutch Stage 1 Combiotic Infant Milk Formula because it was not approved by the FDA and may contain insufficient iron for vulnerable infants, particularly those born prematurely or with low birth weight.

    Product
    HiPP Dutch Stage 1 Combiotic Infant Milk Formula
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0918-2021·2021-08-25

    Holle Bio Stage 2 Organic Infant Formula Lacks Required FDA Pre-Market Notification

    Able Groupe Inc is recalling Holle Bio Stage 2 Organic Follow-On Infant Milk Formula because required FDA pre-market notifications were not submitted and the product lacks mandatory labeling in English required by federal regulations.

    Product
    Holle Bio Stage 2 Organic Follow-On Infant Milk Formula
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0747-2021·2021-08-25

    Leucovorin Calcium for Injection recalled for lack of sterility assurance

    Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection (350 mg/vial) distributed nationwide because the manufacturer cannot assure the product is sterile. Patients using recalled lot should consult their healthcare provider.

    Product
    Leucovorin Calcium for Injection, USP 350 mg/vial, 17.5 mL single-use vials, Rx only, Manufactured by: Teva Pharmaceuticals USA, Inc. North Wales, PA 19454, NDC 0703-5145-91
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0923-2021·2021-08-25

    Lebenswert Folgemilch Stage 3 Organic Toddler Formula Recalled

    Able Groupe Inc is recalling Lebenswert Folgemilch Stage 3 Organic Toddler Formula because required FDA pre-market notifications were not submitted and the product lacks mandatory labeling in English as required by federal regulations.

    Product
    Lebenswert Folgemilch Stage 3 Organic Toddler Formula
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0872-2021·2021-08-25

    Ballreich Barbeque Marcelled Potato Chips Salmonella Contamination Recall

    Ballreich Snack Food Company is recalling Barbeque Marcelled Potato Chips in 1.5, 2.5, and 7 ounce packages due to possible Salmonella contamination from an ingredient. The affected products were distributed in Indiana, Michigan, and Ohio.

    Product
    Barbeque Marcelled Potato Chips Ballreich Snack Food Company 1.5, 2.5, and 7 ounce flexible plastic packaging 1.5 ounce/72 case, 2.75 ounce 32/case, 7 ounce 14/case
    Category
    Food
    Distribution
    3 states
  • SevereUSDA FSIS·029-2021·2021-08-24

    Willow Tree Poultry Farm Recalls Chicken Salads and Dips Due to Plastic Contamination

    Willow Tree Poultry Farm is recalling approximately 52,022 pounds of chicken salads and dips that may contain hard white plastic. The products were distributed to nine northeastern states.

    Product
    WILLOW TREE POULTRY FARM, INC. — Willow Tree Poultry Farm Recalls Chicken Salad and Dip Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    9 states