The Recall Desk

State

Missouri product recalls

72,913 recalls have nationwide distribution and so reach Missouri. 8,461 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,461
Critical
1,333
Severe
1,870
Most recent
2026-09-09

Of the 8,461 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 1,870 (22%) are Severe.

These figures cover only the 8,461 recalls whose distribution notice names Missouri specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1726–1750 of 81374

  • HighFDA (Food)·H-0854-2026·2026-06-03

    Fly By Jing creamy sesame noodles may contain undeclared peanut

    Fly By Jing Creamy Sesame Noodles are being recalled because possible cross-contamination resulted in an undeclared peanut allergen. 3,419 cases are affected.

    Product
    Fly By Jing (branded) Creamy Sesame Noodles; 3.8 oz packets. Sold in single and 4 packs. Single UPC: 8-50052-23988-6 4 pack UPC: 8-50052-23991-6
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2239-2026·2026-06-03

    HydroMARK breast biopsy markers may carry the wrong inner labeling

    HydroMARK Breast Biopsy Site Markers are being recalled because boxes labeled as T3 markers may contain individual packages labeled as T4 markers. 1,910 units are affected.

    Product
    HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2259-2026·2026-06-03

    Philips Allura system hard drives may degrade and lose imaging

    Philips Allura Xper interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.

    Product
    Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013), Allur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V361000·2026-06-03

    Jayco Recalls 2026 Recreational Vehicles Due to Taillight Warning Light Defect

    Jayco is recalling 2026 Entegra and Jayco recreational vehicles because the taillight warning light may illuminate incorrectly, potentially confusing drivers and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO CONDOR, QWEST SE, GRANITE RIDGE, MELBOURNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2258-2026·2026-06-03

    Philips Azurion system hard drives may degrade and lose imaging

    Philips Azurion interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.

    Product
    Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0551-2026·2026-06-03

    Pred Mild prednisolone eye suspension failed stability specifications

    Pred Mild prednisolone acetate ophthalmic suspension 0.12% is being recalled after failing stability specifications. 2,736 bottles are affected.

    Product
    PRED MILD — PRED MILD (PREDNISOLONE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2240-2026·2026-06-03

    Medtronic 1x4 pocket adaptor kits carry incorrect use-by dates

    Medtronic 1x4 Pocket Adaptor Kits for Deep Brain Stimulation, model 64001, are being recalled because a limited number are labeled with incorrect use-by dates. 275 units are affected.

    Product
    Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2241-2026·2026-06-03

    Medtronic 2x4 pocket adaptor kits carry incorrect use-by dates

    Medtronic 2x4 Pocket Adaptor Kits for Deep Brain Stimulation, model 64002, are being recalled because a limited number are labeled with incorrect use-by dates.

    Product
    Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V356000·2026-06-02

    Kia Recalls 2027 Telluride Models for Seat Belt Retraction Defect

    Kia is recalling 2027 Telluride and Telluride Hybrid vehicles because the driver seat belt may fail to extend, increasing injury risk in a crash.

    Product
    KIA — KIA TELLURIDE HYBRID, TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V358000·2026-06-02

    Chrysler Recalls Pacifica and Voyager Models Due to Air Bag Defect

    Chrysler is recalling 2023-2026 Pacifica and Voyager vehicles because a spring may prevent air bags from deploying, increasing injury risk.

    Product
    CHRYSLER — CHRYSLER PACIFICA, VOYAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V355000·2026-06-02

    Nova Bus Recalls LFS Transit Buses Due to Brake Warning Light Defect

    Nova Bus is recalling LFS and LFS Artic transit buses because the low brake air pressure warning light may fail to illuminate when the engine is off, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V352000·2026-05-29

    Forest River travel trailer fireplace outlets may have incorrect wiring

    Forest River is recalling certain 2024-2026 Wildwood and Salem travel trailers because the fireplace outlet may have incorrect wiring, increasing the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM, STEALTH EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V353000·2026-05-29

    2026 Mercedes-Benz and Maybach Models Rear Seat Belt Recall

    Mercedes-Benz USA is recalling 2026 GLS, GLE, and Maybach models due to rear seat belt bolts that may not be properly tightened, reducing restraint effectiveness in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH, MERCEDES BENZ GLE 450 4MATIC, GLS 600 4MATIC, GLE 350, GLE 350 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·26515·2026-05-28

    Anzmtosn Luminous Fidget Spinner Balls Recalled for Battery Ingestion Risk

    Anzmtosn Luminous Fidget Spinner Balls are recalled because the included mini flashlight contains easily accessible button cell batteries that can cause serious internal injuries or death if swallowed by children.

    Product
    Anzmtosn Luminous Fidget Spinner Balls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26508·2026-05-28

    MiniWarGaming and Primal Horizon Disc Magnets Violate Mandatory Safety Standard

    MiniWarGaming Inc. and Primal Horizon are recalling approximately 22,624 disc magnets that violate mandatory safety standards. The high-powered magnets pose a deadly ingestion hazard to children.

    Product
    MiniWarGaming and Primal Horizon Disc Magnets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26506·2026-05-28

    Giantex and Costway Portable Steam Saunas Recalled for Burn Hazard

    Giantex and Costway portable steam saunas are recalled because the steam diffuser can position too close to the user's body, causing burns. Giantex has received nine burn reports, including one second-degree burn.

    Product
    Giantex and Costway 2-liter and 3-liter Portable Steam Saunas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V348000·2026-05-28

    IC Bus Recalls 2026-2027 EVSB School Buses for Drive Motor Bolt Issue

    International Motors is recalling 2026-2027 IC Bus EVSB school buses because improperly tightened bolts may allow the drive motor to detach, creating a road hazard.

    Product
    IC BUS — IC BUS EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V351000·2026-05-28

    Mack Trucks Recalls 644 Vehicles Due to Wheel Lug Nut Loosening Risk

    Mack Trucks is recalling 644 vehicles because wheel lug nuts may loosen, allowing the wheel to detach. Owners are advised not to drive until repairs are completed.

    Product
    MACK — MACK GRANITE (GR), ANTHEM AN (4), PINNACLE (PI/PN), ANTHEM (AN)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26522·2026-05-28

    Walmart recalls Mainstays 9-drawer fabric dressers due to tip-over hazard

    Walmart is recalling about 165,000 Mainstays 9-Drawer Fabric Dressers because they can tip over and cause entrapment if not anchored to a wall, creating a risk of serious injury or death to children.

    Product
    Mainstays 9-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26512·2026-05-28

    Giantex Outdoor Lounge Chairs Recalled Due to Amputation Hazard

    Giantex outdoor lounge chairs model NP10025NY pose an amputation risk when adjusting the backrest due to exposed pinch points. One finger amputation has been reported.

    Product
    Giantex outdoor lounge chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26514·2026-05-28

    Misco Sports Light-Up Racket Sets Recalled for Battery Ingestion Risk

    Missry Associates recalls Misco Sports Light-Up Racket Sets (model MT2287) because the battery compartment screw can detach and button cell batteries in the shuttlecock can be easily accessed by children, posing risk of serious injury or death if swallowed.

    Product
    Misco Sports Light-Up Racket Sets, model MT2287
    Category
    Consumer Product
    Distribution
    Distributed nationwide