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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276–300 of 39702

  • SevereNHTSA·26V603000·2026-09-21

    Forest River Recalls 2026-2027 Dynamax Grand Sport GT Recreational Vehicles

    Forest River is recalling 2026-2027 Dynamax Grand Sport GT recreational vehicles because an improperly installed engine pre-heat pump may cause coolant hose failure and engine overheating.

    Product
    DYNAMAX — DYNAMAX GRAND SPORT GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26779·2026-09-17

    LANCHEZ Pressure Washers Recalled for Shock and Electrocution Hazards

    LANCHEZ pressure washers are recalled because they lack a ground-fault circuit-interrupter and adequate power cord, posing risks of shock or electrocution.

    Product
    LANCHEZ Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V599000·2026-09-17

    Jaguar Land Rover Recalls Vehicles for DC-DC Converter Defect

    Jaguar Land Rover is recalling specific 2019-2024 models because a DC-DC converter malfunction can cause loss of drive power and lighting, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER, JAGUAR RANGE ROVER SPORT, RANGE ROVER VELAR, E-PACE, RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26784·2026-09-17

    Sauna360 Recalls Infrared Saunas Due to Fire and Burn Hazards

    Sauna360 is recalling infrared and hybrid saunas because panels can short circuit and overheat, posing fire and burn risks.

    Product
    Infrared Saunas, Hybrid Infrared Saunas and Infrared Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26777·2026-09-17

    Hayward Recalls Universal Pool Heaters Due to Carbon Monoxide Risk

    Hayward Industries is recalling 400,000 BTU Universal-HC Series pool heaters because they can produce high levels of carbon monoxide, posing a risk of serious injury or death.

    Product
    400,000 BTU Universal-HC Series Pool Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0869-2026·2026-09-16

    B. Braun Recalls Sodium Chloride Injection Due to Particulate Matter

    B. Braun Medical Inc. is recalling 0.9% Sodium Chloride Injection due to the presence of particulate matter, including iron oxide and fibers.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1330-2026·2026-09-16

    FDA Recalls Gluten-Free Veggie Chips for Undeclared Wheat

    Exotique Foods Canada is recalling Momchipz Gluten Free Veggie Chips due to undeclared wheat. The product was sold in the U.S. and poses a risk to individuals with wheat allergies.

    Product
    Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower, net wt. 3oz (85g). UPC 6 28634 44216 6. Ingredients: Broccoli, Cauliflower, Tapioca Flour, Coconut Oil, Salt, White Pepper. Proudly Made in Indonesia. Imported for Exotique Foods, Inc. Toronto, ON - Canada.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-3107-2026·2026-09-16

    Medical Action Industries Recalls Single Shot Epidural Kits Due to Sterility Concerns

    Medical Action Industries is recalling Single Shot Epidural kits containing Sodium Chloride ampules due to potentially compromised sterility.

    Product
    Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
    Category
    Medical Device
    Distribution
    6 states
  • CriticalFDA (Drugs)·D-0865-2026·2026-09-16

    American Regent Recalls Epinephrine Vials Due to Particulate Matter

    American Regent, Inc. is recalling 31,935 vials of Epinephrine Injection due to the presence of particulate matter and broken vials.

    Product
    EPINEPHRINE — EPINEPHRINE (EPINEPHRINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1341-2026·2026-09-16

    International Sprout Holdings Recalls Alfalfa for Potential E. coli and Salmonella

    International Sprout Holdings is recalling 50 lb. bags of alfalfa due to potential E. coli and Salmonella contamination. The product was distributed to wholesale consignees in 16 states, Puerto Rico, and several international locations.

    Product
    Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506
    Category
    Food
    Distribution
    17 states
  • SevereNHTSA·26V596000·2026-09-16

    Rewaco Recalls Three-Wheeled Motorcycles Due to Rear Shock Absorber Defect

    Rewaco is recalling 106 three-wheeled motorcycles because a rear shock absorber connection may loosen, potentially causing a loss of vehicle control.

    Product
    Rewaco — Rewaco RF1 ST-3 Touring, RF1 GT Touring, PUR3 GT, PUR3 GT Touring
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3133-2026·2026-09-16

    MedicaLyte Liquid Bicarbonate Concentrate Recalled for High Endotoxin Levels

    Nipro Renal Solutions is recalling MedicaLyte Liquid Bicarbonate Concentrate due to high endotoxin levels. The product is used in hemodialysis.

    Product
    MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3106-2026·2026-09-16

    Medical Action Industries Recalls Epidural Kits Due to Compromised Sterility

    Medical Action Industries is recalling Epidural/Pain TQC kits containing Sodium Chloride ampules due to potentially compromised sterility.

    Product
    Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-3136-2026·2026-09-16

    Nipro Citric Complete Liquid Citric Acid Concentrate Recalled for High Endotoxin Levels

    Nipro Renal Solutions is recalling Citric Complete Liquid Citric Acid Concentrate due to high endotoxin levels. The product was distributed in the US and internationally.

    Product
    Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+225(45X)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0850-2026·2026-09-16

    Baxter Recalls Dextrose Injection Bags Due to Stainless Steel Particulate Matter

    Baxter Healthcare is recalling 606 bags of Dextrose Injection, USP, 70% due to the presence of stainless steel particles in the solution.

    Product
    Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1331-2026·2026-09-16

    Crown Farms Dried Suri Cut Recalled for Improper Evisceration

    Euro Foods Group USA NJ Inc is recalling Crown Farms Dried Suri Cut because the dried fish was not properly eviscerated prior to drying.

    Product
    Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-3090-2026·2026-09-16

    Given Imaging Recalls Bravo CF Capsule Delivery Devices Due to Attachment Failure

    Given Imaging is recalling Bravo CF capsule delivery devices because they may fail to attach to the esophagus or detach from the device, posing risks of aspiration and perforation.

    Product
    Bravo CF capsule delivery device, 5-pack, Product Number FGS-0635, Bravo CF capsule delivery device, 1-pack, Product Number FGS-0636. Used to attach a pH monitoring capsule to the esophagus.
    Category
    Medical Device
    Distribution
    Distributed nationwide