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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1876–1900 of 39703

  • CriticalFDA (Food)·H-0136-2026·2025-11-05

    Chocolate nonpareils recalled over an undeclared milk allergen in bulk cases

    Weaver Nut Company is recalling 1,760 cases of semi-sweet chocolate nonpareils with white seeds over an undeclared milk allergen. The FDA has classified the recall as Class I.

    Product
    D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution.
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Devices)·Z-0164-2026·2025-11-05

    InVision operating suite recalled over ice blockage in magnet venting paths

    IMRIS is recalling the InVision 3T Operating Suite because an ice blockage in the Siemens 3 Tesla Vida magnet's venting system could rupture the helium containment system during a quench.

    Product
    IMRIS Operating Suite, InVision 3T Operating Suite, containing Siemens 3 Tesla MRI Magnet, Vida
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0162-2026·2025-11-05

    MRI operating suites with Skyra magnet recalled over venting system blockage

    IMRIS is recalling the IMRIS iMRI 3T S Operating Suite because an ice blockage in the Siemens 3 Tesla Skyra magnet's venting system could rupture the helium containment system during a quench.

    Product
    IMRIS Operating Suite, iMRI 3T S, containing Siemens 3 Tesla MRI Magnet, Skyra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0318-2026·2025-11-05

    Glucose monitoring app recalled because it can terminate and miss alerts

    Dexcom is recalling version 1.15.0 of the G6 and G6 Pro Android CGM app because a software defect can terminate the app, stopping glucose values, alarms and alerts. The FDA classified it Class I.

    Product
    Brand Name: Dexcom G6 Continuous Glucose Monitoring System Product Name: Dexcom G6 and G6 Pro Android US CGM App Model/Catalog Number: SW11678 Software Version: version 1.15.0 Product Description: Dexcom G6 and G6 Pro Android US CGM App SW11678 version 1.15.0 Component…
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·H-0137-2026·2025-11-05

    Frozen carrot bundt cakes recalled over an undeclared wheat allergen

    Doan's Dessert And Coffee is recalling its 4 lb Carrot Bundt Cake over an undeclared wheat allergen in ready-to-eat frozen cakes. The FDA has classified the recall as Class I.

    Product
    Carrot Bundt Cake - Net Weight 4 lbs Contains: Wheat, Soy, Milk, Eggs, Tree Nuts No UPC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0143-2026·2025-11-05

    Veggie spring rolls recalled over undeclared shrimp in retail cartons

    Tai Foong USA is recalling 1,261 cases of Fusia Asian Inspirations Veggie Spring Rolls over undeclared shrimp. The FDA has classified the recall as Class I.

    Product
    Fusia Asian Inspirations brand Veggie Spring Rolls. Net weight: 10 oz (283.5 g).) retail package identified by UPC 4099100222258. Type of packaging: Paperboard carton with inner poly bag; 12 ct corrugated master case. Responsible firm on label: ALDI Inc. Batavia, IL 60510…
    Category
    Food
    Distribution
    23 states
  • CriticalFDA (Food)·H-0168-2026·2025-11-05

    Bulk frozen scrambled eggs recalled over potential Listeria monocytogenes contamination

    Echo Lake Foods is recalling 824 cases, 23,072 pounds, of bulk cage free precooked scrambled eggs over potential Listeria monocytogenes contamination. The FDA classified it Class I.

    Product
    EchoLakeFoods MF 3067 CNFREE Cage Free Precooked IAF Scrambled Eggs Net Wt. 28 lbs. Bulk. Keep Frozen. Manufactured by: Echo Lake Foods, Inc., 2319 Raymond Ave. Franksville, WI 53126.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-0138-2026·2025-11-05

    White chocolate coconut bundt cakes recalled over an undeclared wheat allergen

    Doan's Dessert And Coffee is recalling its 3 lb 12 oz White Chocolate Coconut Bundt Cake over an undeclared wheat allergen. The FDA has classified the recall as Class I.

    Product
    White Chocolate Coconut Bundt Cake - Net Weight 3 lbs 12 oz Contains: Wheat, Soy, Milk, Eggs No UPC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0188-2026·2025-11-05

    Distal access catheters recalled after coating material lifting inside the lumen

    Balt USA is recalling 207 MEGA Ballast Distal Access Platform catheters over a manufacturing defect in which coating material lifts within the catheter's distal lumen. The FDA has classified it Class I.

    Product
    Brand Name: MEGA Ballast Distal Access Platform Product Name: Mega Ballast Model/Catalog Number: MEGABT09180, MEGABT09190, MEGABT091100, MEGABT091110 Software Version: N/A Product Description: The Mega Ballast 091 is designed with a semi-rigid proximal shaft and a highly…
    Category
    Medical Device
    Distribution
    12 states
  • SevereNHTSA·25E073000·2025-11-05

    Bendix Recalls EC80 Electronic Control Units Due to Electrical Noise Issues

    Bendix is recalling specific EC80 Electronic Control Units because electrical noise may cause the unit to malfunction, potentially disabling critical vehicle safety systems.

    Product
    SERVICE BRAKES, AIR:ANTILOCK:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·036-2025·2025-11-04

    Brazilian Taste Recalls Frozen Chicken and Beef Croquettes for Undeclared Sesame

    Brazilian Taste is recalling approximately 4,120 pounds of frozen chicken and beef croquettes because they contain sesame, an undeclared allergen.

    Product
    Brazilian Taste — Brazilian Taste Recalls Frozen Chicken and Beef Croquette Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V748000·2025-10-31

    BMW Recalls 2000-2001 X5 Vehicles Due to Air Bag Inflator Defect

    BMW is recalling 2000-2001 X5 vehicles because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V750000·2025-10-31

    Par Nado Alto Travel Trailers Recalled for Gas Leak Risk

    Par Nado is recalling 2019-2020 Alto travel trailers because aluminum burner tubes may crack, causing a gas leak that could lead to fire.

    Product
    SAFARI CONDO — SAFARI CONDO ALTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V741000·2025-10-30

    Jeep Wrangler and Grand Cherokee 4Xe vehicles fire risk battery recall

    Chrysler is recalling certain 2020–2025 Jeep Wrangler 4Xe and 2022–2026 Grand Cherokee 4Xe vehicles because the high voltage battery may fail internally and cause a vehicle fire while parked or driving.

    Product
    JEEP — JEEP GRAND CHEROKEE, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26058·2025-10-30

    Kayak paddles recalled after 80 reports of breaking during use

    About 700 Werner Stealth and Covert kayak paddles are being recalled after 80 reports of the paddles breaking during use, posing a drowning hazard.

    Product
    Stealth and Covert Kayak Paddles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V742000·2025-10-30

    Smeal Recalls 2024-2026 Aerial Vehicles Due to Hydraulic Hose Defect

    Smeal Holding, LLC is recalling 29 emergency response vehicles because a defective crimp may cause hydraulic hoses to leak, risking injury or fire.

    Product
    SMEAL — SMEAL REAR MOUNT AERIAL, AERIAL, MID MOUNT AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26054·2025-10-30

    Off-road vehicles recalled over alternator cable that can short and ignite

    About 5,130 Polaris Ranger XP 1000 NorthStar off-road vehicles are being recalled because an improperly routed alternator cable can short against the battery; six incidents include one fire.

    Product
    Model Year 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 NorthStar Recreational Off-Road Vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26064·2025-10-30

    Chainsaws recalled because the chain brake may not activate

    About 90,860 Milwaukee Tool M18 FUEL top handle chainsaws are being recalled because the chain brake may not activate; two reports include one lacerated finger.

    Product
    Milwaukee Tool M18 FUELTM Top Handle Chainsaw with either a 12" or 14" bar
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26051·2025-10-30

    Bicycle lights recalled after five battery fires or explosions reported

    About 3,790 Knog Blinder 900 and Blinder 1300 front bicycle lights are being recalled after five reports of the lithium-ion battery catching fire or exploding.

    Product
    Knog Blinder 900 and Blinder 1300 Front Bicycle Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26059·2025-10-30

    Dining chairs recalled after 149 reports of chair legs breaking

    About 54,930 Crate & Barrel Ana Dining Chairs are being recalled after 149 reports of chair legs breaking, including 10 reports of injuries to the head, back, arms and face.

    Product
    Ana Dining Chair
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E071000·2025-10-30

    Honda Recalls 18-Inch Aluminum Alloy Wheels for Civic Vehicles

    Honda is recalling 18-inch aluminum alloy wheels for 2016-2021 Civic vehicles because a manufacturing error may allow them to detach, increasing crash risk.

    Product
    WHEELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V743000·2025-10-30

    Jayco Recalls 2025-2026 Entegra Recreational Vehicles for Slide-Out Defect

    Jayco is recalling 2025-2026 Entegra recreational vehicles because slide-out rooms can deploy while the vehicle is moving, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA ANTHEM, ASPIRE, CORNERSTONE, CORNERSTONE RESERVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0132-2026·2025-10-29

    Shrimp scampi meals recalled over linguine linked to Listeria outbreak

    Demers Food Group is recalling 12,962 cases of Scott & Jon's Shrimp Scampi with Linguine because it contains linguine recalled for Listeria monocytogenes and implicated in an ongoing outbreak.

    Product
    Scott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0070-2026·2025-10-29

    Hemodialysis bloodline sets recalled over micro air bubbles from damaged connectors

    B. Braun is recalling Streamline Bloodline Sets for Dialog because damaged arterial and venous patient connectors may cause micro-air bubbles in the bloodline and air-in-line alarms.

    Product
    Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET FOR DIALOG Model/Catalog Number: SL-2010M2096 Software Version: N/A Product Description: STREAMLINE BLOODLINE SET FOR DIALOG Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide