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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501–525 of 90167

  • SevereNHTSA·26V598000·2026-09-17

    Toyota Recalls 2026 Lexus and Grand Highlander Models for Steering Knuckle Defect

    Toyota is recalling 617 specific 2026 Lexus and Toyota models because front steering knuckles may crack, potentially causing a loss of steering control.

    Product
    TOYOTA — TOYOTA, LEXUS GRAND HIGHLANDER, GRAND HIGHLANDER HYBRID, RX, RX HYBRID
    Category
    Vehicle
    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
  • HighCPSC·26775·2026-09-17

    Esjay Recalls Toddler Busy Board Toys Due to Choking Hazard

    Esjay is recalling toddler busy board toys because red knobs can detach, posing a choking hazard to children under three.

    Product
    Esjay Toddler Busy Board Montessori Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26773·2026-09-17

    Char-Broil Recalls Bistro Pro Electric Grills Due to Electric Shock Risk

    Char-Broil is recalling about 10,605 Bistro Pro Electric Grills because a grounding wire can disconnect, posing an electric shock hazard. No injuries have been reported.

    Product
    Charbroil Bistro Pro Electric Grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26782·2026-09-17

    SHEIN Recalls Pull and Chew Montessori Teething Toys Due to Choking Hazard

    SHEIN is recalling Pull & Chew Montessori Teething Toys because the silicone strings violate safety standards and pose a choking risk. No injuries have been reported.

    Product
    Pull & Chew Montessori Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26780·2026-09-17

    Melissa & Doug Recalls Fire Truck Activity Board Toys Due to Choking Hazard

    Melissa & Doug is recalling about 84,000 Lights & Sounds Fire Truck Activity Board toys sold at Target and Amazon because a fire hose port can detach, posing a choking risk.

    Product
    Lights & Sounds Fire Truck Activity Board
    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
  • HighNHTSA·26V597000·2026-09-16

    Rivian Recalls R1S, R1T, and R2 Vehicles for Rear Camera Obstruction

    Rivian is recalling 2022-2027 R1S, 2022-2026 R1T, and 2027 R2 vehicles because a notification may obstruct the rearview camera image, increasing crash risk.

    Product
    RIVIAN — RIVIAN R2, R1T, R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3110-2026·2026-09-16

    Lutronic DermaV Laser System Recalled for Potential Patient Burn Risk

    Lutronic Corporation is recalling 1,065 DermaV Laser Systems because using higher fluences at 1064nm with current cryogen parameters may cause sparks or loud noise, potentially resulting in patient burns.

    Product
    Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy at wavelengths of 532 nm and 1064 nm through a fiber-optic handpiece. The system may be configured with an Intelligent Cooling Device (ICD) to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide