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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15801–15825 of 31567

  • ModerateFDA (Food)·F-0732-2024·2024-01-24

    Central Market Chicken Broth Recalled for Potential Microbial Contamination

    TreeHouse Foods recalls Central Market 32oz Organic No Salt Added Chicken Broth (lot code 98C06193) for potential microbial contamination affecting 439,240 cases distributed across 41 states.

    Product
    Central Market 32oz Organic No Salt Added Chicken Broth
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Food)·F-0726-2024·2024-01-24

    Organic Chicken Broth Recalled Nationwide for Potential Microbial Contamination

    TreeHouse Foods is recalling multiple brands of organic chicken broth due to potential microbial contamination. Approximately 439,240 cases were distributed across 37 states.

    Product
    Organic Chicken Broth sold under: 365 Organic, 32oz Chicken Broth, Good & Gather, 32oz Organic Chicken Broth Sprouts, 32oz Organic Chicken Broth Natures Promise, 32oz Organic Chicken Stock Market Basket, 32oz Organic Chicken Stock O Organics, 32oz Organic Chicken Broth
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Drugs)·D-0230-2024·2024-01-24

    Freskaro Magnesium Citrate oral solution recalled for bacterial contamination

    Pharma Nobis LLC is recalling Freskaro Magnesium Citrate Oral Solution (Grape Flavor) nationwide due to the presence of Acetobacter nitrogenifigens bacteria.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - GRAPE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0722-2024·2024-01-24

    Chicken Broth Recalled for Potential Microbial Contamination

    TreeHouse Foods is recalling 439,240 cases of chicken broth products sold under multiple brands for potential microbial contamination. Products were distributed across 37 states.

    Product
    Chicken Broth sold under Chef's Cupboard, 32oz Chicken Stock, UPC: 4099100067699, carton Gold Emblem, 32oz Chicken Broth, UPC: 50428430095, carton H-E-B, 48oz Chicken Broth, UPC: 41220610013, carton HEB Select Ingredients, 32oz Chicken Broth, UPC: 41220610006, 41220610075 (cl
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Devices)·Z-0736-2024·2024-01-24

    BD PosiFlush Prefilled Saline Syringes Recalled for Incorrect Stopper

    Becton Dickinson is recalling 5,085,120 BD PosiFlush Prefilled Saline Syringes due to an incorrect stopper that increases injection force and may trigger pump alarms.

    Product
    PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0737-2024·2024-01-24

    V. Mueller Bandage Scissors recalled for pink dye staining on handles

    Steris Corporation is recalling V. Mueller Universal Bandage Scissors (Model SU2014-001) due to an incorrect resin carrier in the handle cover. Pink dye residue may appear on scissors and sterilization pouches after processing.

    Product
    V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty, Autoclavable, Overall Length 7 (18 cm)- Intended to cut through tape and bandages Model: SU2014-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·24084·2024-01-18

    Home Design Upholstered Low Profile Beds Recalled for Fall Injury Risk

    Home Design is recalling about 527,177 upholstered low-profile beds sold through Wayfair, Walmart.com, and Overstock.com from July 2018 through November 2023. The beds can break, sag, or collapse during use, creating a fall and injury hazard.

    Product
    Upholstered Low Profile Standard and Platform Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24086·2024-01-18

    Steamist Wall-Mounted Tilt-Up Bath Shower Seats Recalled for Fall and Laceration Hazards

    Steamist is recalling about 3,900 wall-mounted, folding teak wood shower seats because the support rods and mounting brackets can corrode and break, creating fall and laceration hazards. The firm has received 62 reports of the seats breaking, including 4 injury reports.

    Product
    Tilt-Up Bath & Shower Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24085·2024-01-18

    Bokser Home 100% Cotton Mattress Pads Recalled for Fire Hazard

    Bokser Home is recalling about 2,300 units of 100% cotton mattress pads because they violate federal flammability regulations and pose a fire hazard. No injuries have been reported.

    Product
    Bokser Home 100% Cotton Mattress Pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0700-2024·2024-01-17

    Eban's Bakehouse Turtle Brownie Cookies Recalled for Undeclared Milk and Soy

    Eban's Bakehouse LLC is recalling Turtle Brownie cookies that contain undeclared milk and soy allergens. Consumers with allergies should not consume the product.

    Product
    Eban's Bakehouse Sweet Indulgences - Turtle Brownie (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0696-2024·2024-01-17

    Eban's Bakehouse cookies recalled for undeclared milk and soy allergens

    Eban's Bakehouse Sweet Indulgences Brown Butter Snickerdoodles are recalled due to undeclared milk and soy allergens. The FDA Class I recall affects 876 units distributed to 33 states.

    Product
    Eban's Bakehouse Sweet Indulgences - Brown Butter Snickerdoodle (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0694-2024·2024-01-17

    Eban's Bakehouse Sweet Indulgences cookies recalled for undeclared milk and soy

    Eban's Bakehouse LLC is recalling Sweet Indulgences cookies for containing undeclared milk and soy allergens, which pose serious health risks to allergic consumers.

    Product
    Eban's Bakehouse Sweet Indulgences - Variety Pack (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0704-2024·2024-01-17

    Peanut Butter Fudge Recalled for Undeclared Egg Allergen

    All lots of Peanut Butter Fudge sold in Iowa are recalled due to undeclared egg allergen. The manufacturer initiated the voluntary recall.

    Product
    Peanut Butter Fudge, 8oz, packaged in clear, plastic clamshell.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0697-2024·2024-01-17

    Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens

    Eban's Bakehouse has recalled Sweet Indulgences Chocolate Chili Coconut cookies due to undeclared milk and soy allergens. The product was distributed nationwide and poses a risk to allergic consumers.

    Product
    Eban's Bakehouse Sweet Indulgences - Chocolate Chili Coconut (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0703-2024·2024-01-17

    Maple Nut Fudge Recalled Due to Undeclared Egg Allergen

    Valley View Candies is recalling Maple Nut Fudge 8oz containers due to undeclared egg allergen. The product was distributed to retail stores in Iowa.

    Product
    Maple Nut Fudge, 8oz, packaged in clear, plastic clamshell.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0699-2024·2024-01-17

    Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens

    Eban's Bakehouse Sweet Indulgences cookies are recalled due to undeclared milk and soy allergens not listed on the label. Consumers with allergies to milk or soy should not consume this product.

    Product
    Eban's Bakehouse Sweet Indulgences - Peanut Butter Chocolate Chunk (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0695-2024·2024-01-17

    Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens

    Eban's Bakehouse Sweet Indulgences cookies are being recalled due to undeclared milk and soy allergens. Consumers with allergies should not consume these products and should discard or return them.

    Product
    Eban's Bakehouse Sweet Indulgences - Brown Butter Honey Pistachio (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Drugs)·D-0220-2024·2024-01-17

    Prescription Vigabatrin Powder Recalled for Defective Container Leakage Risk

    InvaGen Pharmaceuticals recalls Vigabatrin for Oral Solution nationwide due to defective containers that may leak. Consumers with affected lot should contact their pharmacy or healthcare provider.

    Product
    VIGABATRIN — VIGABATRIN (VIGABATRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0701-2024·2024-01-17

    FDA recalls Chocolate Fudge for undeclared egg allergen

    Valley View Candies recalled Chocolate Fudge due to undeclared egg allergen. The recall affects 348 containers distributed to retail stores in Iowa.

    Product
    Chocolate Fudge, 8oz, packaged in clear, plastic clamshell.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0698-2024·2024-01-17

    Eban's Bakehouse Lemon Sugar Cookies Recalled for Undeclared Milk and Soy

    Eban's Bakehouse Sweet Indulgences lemon cookies are being recalled due to undeclared milk and soy allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    Eban's Bakehouse Sweet Indulgences - Lemon Sugar Cookie/Lemon Shortbread (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • HighFDA (Devices)·Z-0683-2024·2024-01-17

    Sensis Vibe Hemo Medical Device Software May Crash

    Siemens is recalling 331 units of the Sensis Vibe Hemo medical device due to a potential software crash in its documentation functionality application. Units affected are distributed in California, Connecticut, and Florida.

    Product
    Sensis Vibe Hemo
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0705-2024·2024-01-17

    Cardiac Stress Testing System may produce distorted electrocardiogram readings

    The Q-Stress Cardiac Stress Testing System version 6 may distort electrocardiogram (ECG) readings when the Source Consistency Filter is enabled. Healthcare facilities should verify ECG readings and consult product documentation.

    Product
    Q-Stress Cardiac Stress Testing System, version 6, with below product name / product codes: a) QS6 AM12Q KIT AHA XML / QS6-BXXCS: b) QS6 AM12Q KIT BCRT IEC / QS-6CC-DGCXX: c) QS6 AM12Q KIT Z200 BCRT IEC / QS-6CC-DFCXX: d) QS6 AM12Q RS SYS AHA XML / QS-6JB-AXAXA: e) QS6 AM12Q
    Category
    Medical Device
    Distribution
    0 states