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 deaths or serious injuries are reported, 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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

10551–10575 of 31360

  • LowFDA (Food)·F-0113-2025·2024-11-13

    MySyrup Sugar Free Coconut Syrup Recalled for Missing Production Records

    My Chai Inc is recalling 297 jugs of MySyrup Sugar Free Coconut Syrup nationwide due to missing production records. Consumers should not use the product.

    Product
    MySyrup Sugar Free Coconut Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural flavor, potassium sorbate and sodium benzoate (to protect flavor), sucralose, acesulfame potassium, citric acid. Made
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0112-2025·2024-11-13

    MySyrup Sugar Free Caramel Syrup Recalled for Missing Production Records

    My Chai Inc is recalling MySyrup Sugar Free Caramel Syrup (604 jugs, nationwide distribution) due to missing production records that prevent verification of proper processing.

    Product
    MySyrup Sugar Free Caramel Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural flavor, potassium sorbate and sodium benzoate (to protect flavor), sucralose, acesulfame potassium, citric acid. Made b
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0033-2025·2024-11-13

    OTC Cold and Cough Medication Recalled Due to Crystallization

    Denison Pharmaceuticals recalls Maximum Strength Cough and Chest Congestion and Nighttime Severe Cold and Flu Combo Pack due to crystallization and texture changes in affected bottles.

    Product
    MAXIMUM STRENGTH COUGH AND CHEST CONGESTION AND NIGHTTIME SEVERE COLD AND FLU COMBO PACK — MAXIMUM STRENGTH COUGH AND CHEST CONGESTION AND NIGHTTIME SEVERE COLD AND FLU COMBO PACK (DEXTROMETHORPHAN HBR, GUAIFENESIN, ACETAMINOPHEN, DOXYLAMINE SUCCINATE)
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Devices)·Z-0288-2025·2024-11-13

    iotaSOFT Plus Drive Unit Recalled Due to Incorrect GTIN Number

    Iotamotion Inc. is recalling the iotaSOFT Plus Drive Unit (Lot #D500330) due to an incorrect GTIN number on the product label. Five devices were distributed in Iowa.

    Product
    iotaSOFT Plus Drive Unit, REF IM-05. The iotaSOFT Insertion System is intended to aid the surgeon in placement of cochlear implant electrode arrays into a radiographically normal cochlea by controlling the speed of implant insertion.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Food)·F-0115-2025·2024-11-13

    MySyrup Sugar Free Madagascar Vanilla Syrup Recalled for Missing Production Records

    My Chai Inc is recalling MySyrup Sugar Free Madagascar Vanilla Syrup nationwide due to missing production records for the acidified product.

    Product
    MySyrup Sugar Free Madagascar Vanilla Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, Madagascar vanilla extract, sodium benzoate and potassium sorbate (to protect flavor), sucralose, acesulfame potassi
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0108-2025·2024-11-13

    MyChai Chai Tea Concentrate Recalled for Missing Production Records

    My Chai Inc is recalling 11,202 jugs of MyChai Chai Tea Concentrate nationwide due to missing production records.

    Product
    MyChai Chai Tea Concentrate Double. Product is packaged in the same square 0.5 gallon HDPE plastic bottles and have volumes of 68 fl oz. Ingredients: Water, Sugar, Organic Black Tea, Organic Spices, Molasses, Vanilla Extract, Citric Acid, Natural Flavors. Made by: MyChai, Inc.
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0109-2025·2024-11-13

    MyChai Chai Tea Concentrate Recalled Due to Missing Production Records

    MyChai Chai Tea Concentrate is being recalled nationwide due to missing production records. The manufacturer could not provide documentation of the product's manufacturing process.

    Product
    MyChai Chai Tea Concentrate Super. Product is packaged in the same square 0.5 gallon HDPE plastic bottles and have volumes of 68 fl oz. Ingredients: Water, Sugar, Organic Black Tea, Organic Spices, Molasses, Vanilla Extract, Citric Acid, Natural Flavors. Made by: MyChai, Inc. 1
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0117-2025·2024-11-13

    MySyrup Sugar Free Raspberry Syrup Recalled Due to Missing Production Records

    My Chai Inc is recalling MySyrup Sugar Free Raspberry Syrup (491 units, 68 fl oz bottles) distributed nationwide due to lack of production records for this acidified food product.

    Product
    MySyrup Sugar Free Raspberry Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural flavor, vanilla extract, sodium benzoate and potassium sorbate (to protect flavor), sucralose, acesulfame potassium,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V761000·2024-11-10

    Hyundai Nexo Hydrogen Pressure Relief Device Defect Creates Fire Risk

    Hyundai is recalling 2019-2024 Nexo vehicles because the hydrogen pressure relief device may fail and leak, creating a fire risk. Owners are advised to park outside until the repair is complete.

    Product
    HYUNDAI — 2020 HYUNDAI NEXO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V669000·2024-11-09

    Tiffin Allegro Bay motorhome subframe truss collapse fire risk recall

    Tiffin is recalling 2022–2025 Allegro Bay motorhomes due to subframe truss collapse that can pinch electrical wiring and cause electrical arcing, increasing fire risk.

    Product
    TIFFIN — 2022 TIFFIN ALLEGRO BAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V593000·2024-11-08

    Volkswagen Recalls 2024 Atlas Cross Sport for Engine Bearing Defect

    Volkswagen is recalling 2024 Atlas and Atlas Cross Sport vehicles because engine bearings may fail, causing engine stalls and increasing the risk of crashes and fires.

    Product
    VOLKSWAGEN — 2024 VOLKSWAGEN ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25036·2024-11-07

    Smart Electric Space Heaters Recalled for Fire and Burn Hazards

    GoveeLife and Govee smart electric space heaters can overheat and pose fire and burn hazards due to non-compliance with UL 1278 safety standards. About 512,500 units are affected.

    Product
    GoveeLife and Govee Smart Electric Space Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25038·2024-11-07

    Portable Lamps Recalled Due to Fire Hazard from Battery Overheating

    About 5,300 Tala Muse Portable Lamps are recalled due to fire hazard from battery overheating. One incident caused property damage; consumers should stop using the lamps and contact Tala for a free replacement bulb.

    Product
    Tala Muse Portable Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25032·2024-11-07

    Guava Roam strollers recalled due to brake failure and fall hazards

    Guava Roam strollers are recalled because the brakes can fail to engage or unexpectedly disengage, posing fall and injury hazards to children. No injuries have been reported.

    Product
    Guava Roam Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25033·2024-11-07

    Baofali 4-in-1 Microfiber Crib Bumpers Recalled for Suffocation Hazard

    Baofali 4-in-1 Microfiber Crib Safety Bumpers sold on Temu.com violate the federal crib bumper ban and pose a suffocation hazard to infants. About 390 units were sold from June through August 2024.

    Product
    Baofali 4-in-1 Microfiber Crib Safety Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25031·2024-11-07

    Kyte Baby Slumber Suits Recalled Due to Flammability Violation, Burn Injury Risk

    Kyte Baby is recalling about 20,500 Slumber Suits sold from November 2022 to March 2024 because they violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. No injuries have been reported.

    Product
    Kyte Baby Slumber Suits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25034·2024-11-07

    Wolf Dual Fuel ranges with infrared griddles recalled for fire and burn hazards

    Wolf Appliance is recalling about 44,000 Dual Fuel ranges with infrared griddles due to a short-circuit hazard. Liquid spillage can unexpectedly activate the griddle, posing burn and fire risks. No injuries have been reported.

    Product
    Wolf Dual Fuel ranges with infrared griddles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25030·2024-11-07

    Dreamgro Lullaby Travel Soothers Recalled Due to Choking Hazard

    Dreamgro Lullaby mermaid travel soothers are recalled because a gold-colored soft star can detach, posing a choking hazard to infants. No injuries have been reported, but one detachment incident was confirmed.

    Product
    Dreamgro Lullaby mermaid travel soothers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0077-2025·2024-11-06

    Los Andes Foods Sweet Corn Pancakes Recalled for Undeclared Wheat Allergen

    Los Andes Foods Sweet Corn Pancakes are being recalled because they contain undeclared wheat allergen. Consumers with wheat allergies should not consume the product and should discard it.

    Product
    Los Andes Foods Sweet Corn Pancakes, Cachapas de Maiz, NET WT. 24 Oz., 5 units, KEEP REFRIGERATED
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0120-2025·2024-11-06

    Shirakiku Korean Seaweed Recalled for Undeclared Sesame Allergen

    Wismettac Asian Foods recalls Shirakiku Korean Seasoned Seaweed due to incorrect product labeling that fails to disclose sesame. Affected products were distributed in CA, AZ, TX, NM, WA, NY, and NV.

    Product
    The outer package of the recalled product, Shirakiku Korean Seasoned Seaweed Korean Seaweed, is INCORRECTLY labeled as follows: (Principal Display Panel) Roasted Seaweed 10-0.91 OZ (26 G) PACKAGES (NET WT 9.1 OZ (260 G). (Back Display) ROASTED SEAWEED Organic Yaki Nori Ingredient
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-0141-2025·2024-11-06

    GE Healthcare Infant Incubator Recall: Airborne Formaldehyde Off-Gassing

    GE Healthcare Giraffe Incubator Carestation CS1 units may release airborne formaldehyde residue during initial use. Manufacturer notified customers in June 2023 to run incubators for one week to off-gas any residual formaldehyde, which can cause eye irritation.

    Product
    GE Healthcare Giraffe Incubator Carestation CS1, Infant Incubator. Model Numbers: 1) 2082844-002-01040417; 2) 2082844-002-01044956; 3) 2082844-002-01058424; 4) 2082844-002-01069017; 5) 2082844-002-01089666; 6) 2082844-002-01090474; 7) 2082844-002-01091269; 8) 208
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0222-2025·2024-11-06

    Ambulatory Infusion System Batteries May Short Circuit and Overheat

    CADD-Solis battery packs used in ambulatory infusion systems may develop internal short circuits causing battery case melting and charging circuit failure. The FDA Class I recall affects 138,039 units worldwide.

    Product
    CADD-Solis Li-ion Rechargeable Battery Packs, REF 21-2160-XX, which are also sold as a component of the following CADD Solis Ambulatory Infusion Systems: 21-2101-0100-50, 21-2101-0200-02, 21-2101-0200-03, 21-2101-0200-06, 21-2101-0200-07, 21-2101-0200-12, 21-2101-0200-14, 21-210
    Category
    Medical Device
    Distribution
    0 states