The Recall Desk

State

Missouri product recalls

72,820 recalls have nationwide distribution and so reach Missouri. 8,460 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,460
Critical
1,333
Severe
1,869
Most recent
2026-09-02

Of the 8,460 recalls naming Missouri we have scored against our rubric, 1,333 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,869 (22%) are Severe.

These figures cover only the 8,460 recalls whose distribution notice names Missouri specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

326–350 of 81280

  • HighNHTSA·26V531000·2026-08-13

    Chrysler Recalls 2026-2027 Vehicles for Rearview Camera Display Failure

    Chrysler is recalling 2026-2027 Jeep, Ram, Chrysler, and Dodge vehicles because the rearview camera image may fail to display when reversing, increasing crash risk.

    Product
    RAM — RAM, CHRYSLER, JEEP PROMASTER BEV, PACIFICA, 2500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26699·2026-08-13

    SUGIFT Pressure Washers Recalled for Shock and Electrocution Hazards

    SUGIFT is recalling 13 electric pressure washers (Model LTBBHG006) because they lack a ground-fault circuit interrupter and have a short power cord, creating shock and electrocution risks. No injuries have been reported.

    Product
    SUGIFT Electric Pressure Washers, Model LTBBHG006
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26700·2026-08-13

    Zimtown Portable Gas and Fuel Cans Recalled Due to Burn and Child Poisoning Risk

    Fastbuy is recalling about 200 Zimtown portable gas and fuel cans because the spout closure is not child-resistant, posing burn and poisoning risks to children. No injuries have been reported.

    Product
    Zimtown Portable Gas and Fuel Cans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26692·2026-08-13

    COMMOWNER Electric Pressure Washers Recalled Over Shock and Electrocution Hazards

    COMMOWNER electric pressure washers (models HD14P-Z and HX18) are recalled due to shock and electrocution hazards from a missing built-in GFCI. No injuries reported; stop use and contact AZ Home Concept for a refund.

    Product
    COMMOWNER Electric Pressure Washers, model numbers HD14P-Z and HX18
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26697·2026-08-13

    Shengsen Prank Sound Makers Recalled Over Battery Ingestion Risk

    Shengsen Prank Sound Makers are recalled because the lithium coin batteries can be easily accessed by children, posing an ingestion hazard. About 667 units sold on Amazon from April 2024 through April 2026 are affected.

    Product
    Shengsen Prank Sound Maker
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26702·2026-08-13

    Hampton Bay 52-Inch Ceiling Fans Recalled Over Blade Separation Hazard

    Hampton Bay Halwin 52-inch ceiling fans are being recalled because the fan blades can separate from the motor flywheel, posing impact and injury risks. About 9,460 units sold at Home Depot between January 2023 and October 2025 are affected.

    Product
    Hampton Bay Halwin 52-inch Indoor/Outdoor Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26696·2026-08-13

    Ritchey Recalls Carbon Bicycle Forks Due to Fall and Crash Hazard

    Ritchey Design is recalling about 775 carbon bicycle forks because the alloy insert in the crown hole can come loose, letting an accessory fall onto the front wheel and cause a crash. No injuries have been reported.

    Product
    Ritchey Carbon Fiber Bicycle Forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26690·2026-08-13

    DUMOS Nine-Drawer Dressers Recalled for Tip-Over and Entrapment Hazards

    DUMOS Nine-Drawer Dressers are recalled because they can tip over and entrap children if not anchored to the wall, violating the STURDY Act. Consumers should stop using unanchored units and contact DUMOS for a full refund.

    Product
    DUMOS Nine-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26689·2026-08-13

    TooyBing Wooden Bead Stacking Toys Recalled Due to Choking Hazard

    TooyBing is recalling its Wooden Bead Stacking Toys because the wooden beads pose a choking hazard to children under three years old.

    Product
    TooyBing Wooden Bead Stacking Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26695·2026-08-13

    Qabefy Mattresses Recalled Due to Fire Hazard; Violate Flammability Standard

    Qabefy twin mattresses sold on Amazon are recalled because they violate the federal flammability standard, posing a fire hazard. Consumers should stop using them and contact Qabefy for a refund.

    Product
    Qabefy Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26691·2026-08-13

    Deli Jerry Fuel Containers Recalled Due to Burn Hazard and Child Poisoning Risk

    Deli Jerry fuel containers sold on Walmart.com are recalled because their caps are not child-resistant, posing burn and poisoning risks to children. No injuries have been reported; consumers should stop using them and contact Deli OfficeSupplies for a refund.

    Product
    Deli Jerry Fuel Containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26698·2026-08-13

    CuberShop Magnetic Speed Cubes Recalled Over Magnet Ingestion Hazard

    CuberShop Magnetic Stickerless Speed Cubes (model YJ MGC 5×5) are recalled because loose high-powered magnets in the packaging pose an ingestion hazard to children. No injuries have been reported.

    Product
    CuberShop Magnetic Stickerless Speed Cubes, model YJ MGC 5×5
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V530000·2026-08-13

    GM Recalls 2024-2025 Silverado and Sierra 2500 Tires

    General Motors is recalling 2024-2025 Chevrolet Silverado 2500 and GMC Sierra 2500 trucks because incorrect tire pressure labels may cause underinflation and prevent low-pressure warnings.

    Product
    GMC — GMC, CHEVROLET SIERRA 2500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2797-2026·2026-08-12

    Halyard Convenience Kits Recalled Due to Particulates in Manifolds

    AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.

    Product
    Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. SAMMC ANGIOGRAPHY SAMM066-15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0743-2026·2026-08-12

    Cyclophosphamide Injection Recalled Due to Stainless Steel Particulate Matter

    Sunny Pharmtech Inc. is recalling 4,077 vials of Cyclophosphamide for Injection due to stainless steel particulate matter found in the product. The recall affects vials distributed nationwide in the USA.

    Product
    Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2796-2026·2026-08-12

    Halyard convenience kits recalled due to potential particulates in manifolds

    AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.

    Product
    Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2856-2026·2026-08-12

    Powered Wheelchair Control Software Recall by munevo

    Munevo is recalling 19 powered wheelchair hands-free control systems due to a software issue that may cause the driving mechanism to fall out of calibration, leading to unexpected steering drift or imprecise control.

    Product
    munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2835-2026·2026-08-12

    Therabody Theragun G4 PRO Charger Recalled for Fire Risk

    Therabody is recalling Theragun G4 PRO chargers because they may overheat, presenting a risk of fire, smoke, or melting.

    Product
    Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO charger. G4 PRO Black US - Refurb., SKU TG02428-01 G4 PRO NA, SKU G4-PRO-PKG-NA G4-PRO-PKG-US, SKU G4 PRO US G4 PRO Black US - Refurb V, SKU TG0002428
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V525000·2026-08-12

    BMW Vehicles Recalled Due to Potential Loss of Power and Rollaway Risk

    BMW is recalling certain 2021–2026 BMW models because the connection between the driveshaft and rear differential may become damaged, potentially causing a loss of power or vehicle rollaway.

    Product
    BMW — BMW 750E XDRIVE, 840I, 840I XDRIVE, 540I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2854-2026·2026-08-12

    Copan WASPLab Software Recall Over Results Overwrite Issue

    Copan WASP is recalling WASPLab devices due to a software issue in the WebApp that may prevent users from overwriting results. The recall affects WebApp versions 2.33.1, 2.33.3, and 2.34.2.

    Product
    Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1, 2.33.3 and 2.34.2 Product Description: WASPLab is an automated device intended to be used for the incubation and the digital imaging of agar culture plates streaked w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0745-2026·2026-08-12

    FDA Recalls Mirabegron Tablets Over Nitrosamine Impurity

    Zydus Pharmaceuticals is recalling Mirabegron extended-release tablets, 25 mg, due to an out-of-specification result for the N-Nitroso Mirabegron impurity. The recall affects nationwide distribution in the USA.

    Product
    MIRABEGRON — MIRABEGRON (MIRABEGRON)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2875-2026·2026-08-12

    Merge OrthoPACS Imaging Workstation Recall for Patient Data Display Issue

    Merge Healthcare is recalling 5 units of its Merge OrthoPACS medical imaging diagnostic workstation due to a software issue where thumbnails from a previously opened patient study may appear while a different patient study is currently open.

    Product
    Merge OrthoPACS, medical imaging diagnostic workstation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2857-2026·2026-08-12

    OXOS Medical Recalls MC2 Portable X-Ray Systems Over Circuit Board Overheating

    OXOS Medical Inc is recalling 77 units of the MC2 Portable X-Ray System due to a defective circuit board that overheats. The recall affects devices distributed nationwide in FL, GA, IN, SC, TX, and VA.

    Product
    Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version: 5.7.0 Product Description: The MC2 Portable X-Ray System ( MC2 System or MC2 ) is a portable and handheld x-ray system designed to aid clinicians with po
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2852-2026·2026-08-12

    Quantum Rehab 4Front Powered Wheelchair Controller Software Recall

    Pride Mobility is recalling 1,102 Quantum Rehab 4Front powered wheelchairs with controller software version 2.0.11 due to a defect that may cause unexpected brake stops or control system crashes.

    Product
    Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2862-2026·2026-08-12

    Stryker AHTO Tube Set Packaging Recalled for Handpiece Leaking

    Stryker is recalling 46,212 units of its AHTO Tube Set Packaging (Catalog Number 0250070600) due to reported complaints of leaking from the handpiece during use. The recall affects products distributed worldwide, including US Nationwide and multiple countries.

    Product
    STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
    Category
    Medical Device
    Distribution
    Distributed nationwide