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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1576–1600 of 39703

  • CriticalFDA (Food)·H-0393-2026·2026-01-21

    Moringa powder recalled over possible contamination with Salmonella Richmond

    Organic Living Superfoods is recalling 88 lbs of Healthy Truth brand Moringa Powder because the products may be contaminated with Salmonella Richmond. The action is Class I.

    Product
    Healthy Truth brand Moringa Powder; 5lb and 20lb
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Devices)·Z-1022-2026·2026-01-21

    Libre 3 Plus sensors, REF 78769-01, recalled over carbon build up

    Abbott Diabetes Care is recalling 258,913 FreeStyle Libre 3 Plus sensors, REF 78769-01, because carbon build up in the sensor may result in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1021-2026·2026-01-21

    Libre 3 Plus sensors recalled in a second lot over carbon build up

    Abbott Diabetes Care is recalling 1,663,241 FreeStyle Libre 3 Plus sensors, REF 78768-01, because carbon build up in the sensor may result in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 78768-01 UDI-DI code: 00357599844011 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Food)·H-0399-2026·2026-01-21

    Plant-based almondmilk chocolate bars recalled over undeclared hazelnut

    Fran's Chocolates is recalling 112 units of Fran's PureBar Almondmilk Chocolate 46% Madagascar over undeclared hazelnut. The FDA has classified the action as Class I.

    Product
    Fran s PureBar Almondmilk Chocolate 46% Madagascar Plant-Based, net wt. 1.1oz, UPC 7 49668 24280 2. Ingredients: Sugar, cocoa butter, cocoa beans, almonds, sunflower lecithin, vanilla extract. May contain traces of milk, peanuts and sesame. Fran's Chocolates, Ltd. Seattle, WA…
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1023-2026·2026-01-21

    Libre 3 Plus sensors recalled over carbon build up causing low readings

    Abbott Diabetes Care is recalling 8,062 FreeStyle Libre 3 Plus sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1020-2026·2026-01-21

    Glucose monitoring sensors recalled over carbon build up causing low readings

    Abbott Diabetes Care is recalling 1,060,723 FreeStyle Libre 3 sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Food)·H-0404-2026·2026-01-21

    Ayurvedic gastro supplement recalled over potential undeclared wheat

    Herbs Forever is recalling 45 units of HerbsForever Gastro Care Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The FDA has classified the action as Class I.

    Product
    HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814 00124 3
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0405-2026·2026-01-21

    Hingwastika churna supplement recalled over potential undeclared wheat

    Herbs Forever is recalling 45 units of HerbsForever Hingwastika Churna Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The action is Class I.

    Product
    HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V024000·2026-01-21

    Ford Recalls 2026 Explorers for Windshield Bonding Defect

    Ford is recalling 2026 Explorer vehicles because the windshield may not be properly bonded, posing an injury risk in a crash.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0402-2026·2026-01-21

    Mandible and ear procedure packs recalled over recalled B. Braun sets

    Medline is recalling 96 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Atwater's, Holiday Cookie Tin, 19.65 ounces, Round metal tin with a window lid
    Category
    Medical Device
    Distribution
    1 state
  • SevereNHTSA·26V023000·2026-01-20

    2025 Nissan Sentra door strikers may fail while vehicle in motion

    Nissan is recalling certain 2025 Sentra vehicles because door strikers may have been improperly welded and could break, allowing doors to open while the vehicle is moving. This increases the risk of injury or crash.

    Product
    NISSAN — NISSAN SENTRA, ALTIMA, KICKS, FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V020000·2026-01-19

    Fifth wheel trailer ramp door may break away from its frame

    Forest River is recalling certain fifth wheel travel trailers across the Work and Play, Coachmen Adrenaline, Chaparral, Riverstone, Takoda, Shasta Phoenix and Cedar Creek ranges because the ramp door may break away.

    Product
    EAST TO WEST — EAST TO WEST, COACHMEN, FOREST RIVER TAKODA, ADRENALINE, RIVERSTONE, WORK AND PLAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·001-2026·2026-01-16

    Suzanna's Kitchen Recalls Grilled Chicken Breast Fillets Due to Listeria Risk

    Suzanna's Kitchen is recalling approximately 13,720 pounds of ready-to-eat grilled chicken breast fillets due to possible Listeria monocytogenes contamination.

    Product
    Suzanna's Kitchen Inc — Suzanna’s Kitchen Recalls Ready-To-Eat Grilled Chicken Breast Fillet Products due to Possible Listeria Contamination
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·26V015000·2026-01-16

    Newmar Recalls 2026 Freedom Aire Motorhomes Due to Fire Risk

    Newmar is recalling 2026 Freedom Aire motorhomes because a water tank heating pad may fail, increasing the risk of a fire.

    Product
    NEWMAR — NEWMAR FREEDOM AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V009000·2026-01-15

    Rivian second-row seat belt retractor bolts may be improperly tightened

    Rivian is recalling certain 2022-2025 R1T and 2022-2026 R1S vehicles because the bolts securing the second-row seat belt retractor assemblies may be improperly tightened.

    Product
    RIVIAN — RIVIAN R1T, R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E003000·2026-01-15

    Ford Recalls Engine Block Heaters Due to Fire Risk

    Ford is recalling specific engine block heaters for 2013-2019 Ford and Lincoln vehicles because they may crack, leak coolant, and cause electrical short circuits that increase fire risk.

    Product
    EQUIPMENT:ELECTRICAL:ENGINE BLOCK HEATER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26199·2026-01-15

    Frigidaire minifridges recalled after at least six caught fire

    About 330,000 Curtis International Frigidaire-brand 6-can minifridges, model EFMIS121, are being recalled after at least six reports of fires with property damage.

    Product
    Frigidaire-brand Minifridges, model EFMIS121, with limited serial numbers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V011000·2026-01-15

    Ford Recalls Focus, Escape, and MKC for Engine Block Heater Fire Risk

    Ford is recalling 2013-2019 Focus, Escape, and 2015-2016 MKC vehicles because a cracked engine block heater may short circuit and cause a fire.

    Product
    LINCOLN — LINCOLN, FORD MKC, FOCUS, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0373-2026·2026-01-14

    Ambriola Piccante pecorino romano recalled after testing positive for Listeria

    Ambriola is recalling 179 bags of Ambriola Piccante grated Pecorino Romano in 5 and 10-pound sizes after the product tested positive for Listeria monocytogenes.

    Product
    Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags (units)
    Category
    Food
    Distribution
    20 states
  • CriticalFDA (Drugs)·D-0288-2026·2026-01-14

    ReBoost nasal spray recalled over yeast, mold and microbial contamination

    MediNatura is recalling all lots within expiry of ReBoost Nasal Spray after the products were found to contain yeast, mold and microbial contamination identified as Achromobacter.

    Product
    REBOOST — REBOOST (SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE AND PULSATILLA VULGARIS)
    Category
    Drug
    Distribution
    Distributed nationwide