The Recall Desk

State

Missouri product recalls

20,096 recalls have nationwide distribution and so reach Missouri. 0 additional recalls listed Missouri specifically in their distribution scope.

About recalls in Missouri

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Missouri consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

7076–7100 of 20096

  • 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 (Food)·F-0118-2025·2024-11-13

    MySyrup Sugar Free Salted Caramel Syrup recalled due to missing production records

    My Chai Inc is recalling MySyrup Sugar Free Salted Caramel Syrup nationwide due to lack of production records documenting acidification procedures.

    Product
    MySyrup Sugar Free Salted 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.
    Category
    Food
    Distribution
    Distributed nationwide
  • 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-0110-2025·2024-11-13

    MyChai Chai Tea Concentrate recalled for missing production records

    My Chai Inc is recalling 19,171 jugs of MyChai Chai Tea Concentrate Original Double distributed nationwide due to missing production records.

    Product
    MyChai Chai Tea Concentrate Original 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: MyCh
    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
  • 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·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·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·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
  • 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
  • SevereFDA (Devices)·Z-0092-2025·2024-11-06

    VasoView HemoPro Vessel Harvesting System Recalled for Silicone Component Detachment

    Maquet Cardiovascular is recalling the VasoView HemoPro Endoscopic Vessel Harvesting System due to silicone detachment from the Harvesting Tool Jaws during use. This FDA Class I recall affects 28,809 units worldwide.

    Product
    VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0244-2025·2024-11-06

    Surgical patties and strips recalled for elevated endotoxin levels in raw materials

    Integra LifeSciences has recalled Codman surgical patties and strips due to higher-than-expected endotoxin levels in raw materials, which may result in out-of-specification endotoxin in finished products.

    Product
    SURG PAT XRAY 1/2X2 Model/Catalog Number: 801406. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0235-2025·2024-11-06

    Surgical Patties and Strips Recalled for Elevated Endotoxin Levels

    Integra LifeSciences is recalling CODMAN Surgical Patties and Strips due to higher-than-expected endotoxin levels in raw material that may result in out-of-specification endotoxin in finished products.

    Product
    MICR PATIE RND Model/Catalog Number: 801396. CODMAN Surgical Patties and CODMAN Surgical Strips are manufactured of COTTONOID¿ Material with x-ray detectable markers. All patties have a suture string attached for ease in performing postsurgical count verification. The surgical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V441000·2024-11-06

    Volvo Trucks Recall for Loose Steering Gear Fasteners

    Volvo Trucks is recalling 2023-2024 VN, VHD, and VAH trucks because steering gear fasteners may not be properly tightened, risking loss of vehicle control. Dealers will tighten the fasteners at no cost to owners.

    Product
    VOLVO — 2023 VOLVO VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V439000·2024-11-06

    2023 Lincoln Nautilus Brake System Risk from Defective Rear Shock Absorbers

    Ford is recalling 366 2023 Lincoln Nautilus vehicles due to incorrectly manufactured rear shock absorbers that may damage the brake hose, potentially extending stopping distance and increasing crash risk. Dealers will inspect and replace affected components at no cost.

    Product
    LINCOLN — 2023 LINCOLN NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0241-2025·2024-11-06

    Surgical Patties and Strips Recalled for Elevated Endotoxin Levels

    Integra LifeSciences Corp. is recalling surgical patties and strips (Model 801402) used in surgery due to higher-than-expected endotoxin levels in raw materials that may affect the finished product.

    Product
    SURG PAT XRAY 1/2X1 Model/Catalog Number: 801402. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0274-2025·2024-11-06

    FDA Recalls Pediatric Oropharyngeal Airway Kit for Regulatory Non-Compliance

    King Systems Corp. is recalling 21,591 KING LTSD airway kits nationwide. The devices were distributed with an unauthorized indication for pediatric use that exceeds FDA regulatory authorization.

    Product
    KING LTSD,SIZE 1, W/SUCTION PORT NON-STERILE KIT-Inserted into a patient s pharynx through the mouth to provide patent airway. Model/Catalog Number: KLTSD431
    Category
    Medical Device
    Distribution
    Distributed nationwide