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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17701–17725 of 39601

  • CriticalFDA (Drugs)·D-1000-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Green MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1004-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Purple 8-1, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1006-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Red Borneo, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1012-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, White Horn, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1002-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Plantation Red MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1652-2018·2018-07-18

    Peanut Processors Recalls Dry Roasted Peanut Granules Due to Salmonella

    Peanut Processors, Inc. is recalling dry roasted peanut granules after a customer reported the product tested positive for Salmonella.

    Product
    DRY ROASTED MEDIUM CHOP PEANUT GRANULES NET WT 30LBS (13.61 KGS) Peanut Processors of Sherman Hwy 87 & Albert Street, Dublin, NC 28332
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1619-2018·2018-07-18

    Brew Dr. Kombucha Recalled Due to Glass Fragments in Bottles

    Brew Dr. Kombucha is recalling Clear Mind kombucha bottles because glass fragments were found inside. Consumers should stop using the affected products.

    Product
    Brew Dr. Kombucha Clear Mind, item Code: FCG0002, 6 glass bottles per case, net volume: 32 FL OZ (946 ML). UPC: 51107 00369. The bottle's label is read in parts: "***CLEAR MIND***INGREDIENTS: Brewed tea (filtered water, organic green tea, organic rosemary, organic peppermint…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-1015-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Yellow Thai, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V478000·2018-07-18

    Freightliner Cascadia Trucks Recalled for Tire Cords Visible Through Innerliner

    Daimler Trucks North America is recalling 2019 Freightliner Cascadia trucks equipped with specific Continental tires because visible cords may cause sudden air loss and loss of vehicle control.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2403-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, LEFT T2 GTN ¿12x360 mm, Product Number 18501236S
    Category
    Medical Device
    Distribution
    8 states
  • SevereNHTSA·18E057000·2018-07-18

    Brembo Recalls Federal Mogul Rear Brake Pads Due to Material Detachment

    Brembo is recalling certain Federal Mogul rear brake pads because the material may detach from the back plate, potentially affecting braking performance.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:PADS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V479000·2018-07-18

    Freightliner Recalls 2019 Cascadia Trucks for Tire Defect

    Daimler Trucks North America is recalling 2019 Freightliner Cascadia trucks equipped with specific Continental tires that may lose air suddenly, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2397-2018·2018-07-18

    Stryker Recalls Specific Femoral Nail Due to Potential Breakage Risk

    Stryker GmbH is recalling specific femoral nails due to potential manufacturing defects that could cause the device to break prematurely.

    Product
    Femoral Nail, A/R T2 Femur ¿15x240 mm, Product Number 18251524S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Drugs)·D-1011-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling White Borneo Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, White Borneo, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2417-2018·2018-07-18

    Medtronic EnTrust ICD Recall for Potential Loss of High Voltage Therapy

    Medtronic is recalling 8,890 EnTrust ICDs due to a potential loss of high voltage therapy near end-of-life. Patients should contact their healthcare provider.

    Product
    Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154ATG Product Usage: The device indicated for use in ICD patients with atrial tachyarrhythmias, or who are at significant risk of developing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2406-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, RIGHT T2 GTN ¿14x460 mm, Product Number 18511446S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2418-2018·2018-07-18

    Medtronic EnTrust ICD Recall for Potential Loss of High Voltage Therapy

    Medtronic is recalling 3 EnTrust ICDs because they may lose high voltage therapy near battery end-of-life without prior warning.

    Product
    Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D153VRC Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2393-2018·2018-07-18

    Stryker Tibial Nail Recall Due to Potential Premature Breakage

    Stryker GmbH is recalling specific Tibial Nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2420-2018·2018-07-18

    Medtronic EnTrust Escudo ICD Recall for Potential Loss of Therapy

    Medtronic is recalling EnTrust Escudo ICDs due to a potential loss of high voltage and anti-tachycardia pacing therapy as the battery nears its end of life.

    Product
    Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V475000·2018-07-18

    Forest River Recalls 2018-2019 Trailers Due to Wheel Bearing Defect

    Forest River is recalling 2018-2019 Rockwood and Flagstaff trailers because inner wheel bearings may seize, causing wheels to lock up and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER FLAGSTAFF, ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2405-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and lead to premature breakage.

    Product
    Femoral Nail, RIGHT T2 GTN ¿9x320 mm, Product Number 18510932S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Food)·F-1615-2018·2018-07-18

    Hee Chang Dairy Black Bean Cereal Latte Recalled for Undeclared Allergens

    Hee Chang Dairy & Food Co., LTD is recalling Black Bean Cereal Latte because FDA inspection found undeclared allergens in the product.

    Product
    Black Bean Cereal Latte; 28.2 oz. package Ingredients: Non Dairy Creamer (corn syrup, vegetable oil, Sodium Caseinate, Silicon dioxide), Rice Powder, Bean Powder, Silicon dioxide, Refined Salt, Black Sesame. Corn syrup 57% Hydrogenated coconut oil 28% Sweet whey powder…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2395-2018·2018-07-18

    Stryker Recalls 17 Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling 17 femoral nails because non-conforming cannulation may reduce component strength and cause premature breakage.

    Product
    Femoral Nail, A/R T2 Femur ¿10x340 mm, Product Number 18251034S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Drugs)·D-1014-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling White Thai Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, White Thai, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2408-2018·2018-07-18

    Stryker Recalls Ankle Arthrodesis Nails Due to Potential Breakage Risk

    Stryker GmbH is recalling specific ankle arthrodesis nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Ankle Arthrodesis Nail, right T2 Ankle ¿11x300mm, Product Number 18191130S
    Category
    Medical Device
    Distribution
    8 states