The Recall Desk

State

Missouri product recalls

73,737 recalls have nationwide distribution and so reach Missouri. 8,500 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,500
Critical
1,339
Severe
2,203
Most recent
2026-10-28

Of the 8,500 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,203 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,500 recalls whose distribution notice names Missouri specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30951–30975 of 82237

  • HighUSDA FSIS·PHA-08012020·2020-08-01

    USDA Alert: Frozen Taquitos and Chimichangas May Contain Hard Plastic

    USDA FSIS issued a public health alert for frozen taquitos and chimichangas that may contain hard plastic from recalled green chilies.

    Product
    Ajinomoto Foods North America — FSIS Issues Public Health Alert for Meat and Poultry Taquitos and Chimichangas Containing FDA-Regulated Diced Green Chilies That Have Been Recalled Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V447000·2020-07-31

    Hyundai Recalls 2020 Genesis G70 for Steering Locking Risk

    Hyundai is recalling 2020 Genesis G70 vehicles because a steering component may be defective, potentially causing the steering to lock or become difficult to operate while driving.

    Product
    HYUNDAI — HYUNDAI GENESIS G70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V449000·2020-07-31

    Mercedes-Benz Recalls Vehicles for Seat Belt Warning Software Defect

    Mercedes-Benz is recalling specific 2017-2019 models because instrument cluster software may cause the seat belt warning system to display a solid light instead of a blinking light with an audible tone.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS 450, E 300, C 300, E 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V450000·2020-07-31

    Autocar Xpeditor Parking Brake May Apply Unexpectedly

    Certain 2018-2021 Autocar Xpeditor right-hand drive trucks may have improperly assembled parking brake plumbing, causing the brake to apply unexpectedly and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E053000·2020-07-31

    Walmart Recalls Hyper Tough 2 Ton Jack Stands Due to Collapse Risk

    Walmart is recalling specific Hyper Tough 2 Ton Jack Stands that may collapse unexpectedly under load, posing a risk of injury to nearby persons.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E052000·2020-07-30

    ZF Recalls Air Bag Crash Sensors in Chrysler and Volkswagen Vehicles

    ZF is recalling air bag crash sensors in 2019 Chrysler Jeep Cherokee and 2018 Volkswagen Atlas vehicles due to manufacturing defects that may delay or prevent air bag deployment.

    Product
    AIR BAGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V446000·2020-07-30

    GM Recalls 2020 Vehicles Due to Roof-Rail Air Bag Defect

    General Motors is recalling 2020 Buick, Cadillac, Chevrolet, and GMC vehicles because the roof-rail air bag inflator may separate during deployment, increasing injury risk.

    Product
    GMC — GMC, CHEVROLET, CADILLAC SIERRA 1500, SILVERADO 3500, SILVERADO 1500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1408-2020·2020-07-29

    Mystic Shield Hand Sanitizer Recalled for Undeclared Methanol

    Transliquid Technologies is recalling Mystic Shield hand sanitizer bottles due to the presence of undeclared methanol.

    Product
    Mystic Shield PROTECTION, ALCOHOL ANTISEPTIC 70%, Topical Solution, Antiseptic Hand Rub, Non-sterile Solution, Extra strength Formula*, 8.45 fl. oz. (250 ml) bottle, Labeled with green or blue labels, Manufactured by Mystic Intl S.A. de C.V. UPC barcode: 7 87790 33952 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2676-2020·2020-07-29

    Boston Scientific Recalls IcePearl Cryoablation Needles Due to Surface Deterioration

    Boston Scientific is recalling 48 IcePearl 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IcePearl 2.1 CX Needle Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2643-2020·2020-07-29

    Wellspect Recalls LoFric Origo Urinary Catheters Due to Tip Defect

    Wellspect HealthCare is voluntarily recalling specific LoFric Origo urinary catheters because of a potential defect in the distal tip.

    Product
    LoFric Origo, Nelaton, 16in, FR10 urinary catheters
    Category
    Medical Device
    Distribution
    22 states
  • HighFDA (Devices)·Z-2674-2020·2020-07-29

    Boston Scientific Recalls IcePearl Cryoablation Needles Due to Surface Deterioration

    Boston Scientific is recalling IcePearl 2.0 CX 90 Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IcePearl 2.0 CX 90 Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2673-2020·2020-07-29

    Medtronic Xomed IPC Software Upgrade Recalled for Speed Control Issue

    Medtronic Xomed is recalling IPC software upgrade v 2.7.3.0 because the M5 Microdebrider may rotate faster than the set value.

    Product
    Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal, drilling and sawing of soft and hard tissue and bone in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V442000·2020-07-29

    Fleetwood Pace Arrow Motorhomes Recalled for Battery Fire Risk

    REV Recreation Group is recalling 2019-2020 Fleetwood Pace Arrow motorhomes because loose battery brackets may cause a short circuit and fire.

    Product
    FLEETWOOD — FLEETWOOD PACE ARROW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2678-2020·2020-07-29

    Boston Scientific Recalls IceFORCE Prostate Kit Due to Needle Surface Deterioration

    Boston Scientific is recalling 79 IceFORCE 2.1 CX Prostate Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IceFORCE 2.1 CX Prostate Kit Visual ICE System, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2680-2020·2020-07-29

    Boston Scientific Recalls Prostate Cryoablation Kits Due to Needle Deterioration

    Boston Scientific is recalling 88 Prostate Cryoablation Kits because needle surfaces deteriorated during procedures due to unexpected electrolysis.

    Product
    Ablation Galil Technology, Three IceFORCE 2.1 CX Prostate Cyroablation Kit Visual ICE System, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2679-2020·2020-07-29

    Boston Scientific Recalls IcePearl 2.1 CX Prostate Kit Due to Needle Deterioration

    Boston Scientific is recalling 193 IcePearl 2.1 CX Prostate Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IcePearl¿2.1 CX Prostate¿Kit Visual Ice System, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2682-2020·2020-07-29

    Boston Scientific Recalls IcePearl Cryoablation Needles Due to Surface Deterioration

    Boston Scientific is recalling 205 IcePearl 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IcePearl 2.1 CX 90 Cyroablation Needles, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2689-2020·2020-07-29

    Philips IntelliVue G7m Anesthesia Gas Module Firmware Recall

    Philips is recalling 3,075 IntelliVue G7m Anesthesia Gas Modules due to a firmware issue that may interrupt gas measurement and display.

    Product
    IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00, System Codes 453564477391, 453564477401, 866173
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2640-2020·2020-07-29

    EHOB Expansion Control Overlay Recalled for Potential Blood Contamination

    EHOB, Inc. is recalling 173 Expansion Control Overlays (Item No. 1004EC) because a portion of the lot may have been contaminated with blood.

    Product
    Expansion Control Overlay, Item No. 1004EC - Product Usage: The EHOB WAFFLE Overlay is more than a support surface, assisting in lateral transfers, boosts and turns to protect patients throughout the hospital journey. Through immersion and envelopment, the WAFFLE Overlay is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2677-2020·2020-07-29

    Boston Scientific Recalls IceFORCE 2.1 CX Cryoablation Needles

    Boston Scientific is recalling 39 IceFORCE 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IceFORCE 2.1 CX Needle Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide