The Recall Desk

State

Missouri product recalls

73,809 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,501
Critical
1,339
Severe
2,204
Most recent
2026-11-04

Of the 8,501 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 2,204 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41001–41025 of 82310

  • ModerateFDA (Devices)·Z-2767-2018·2018-09-26

    Foley Catheter with Temperature Sensor Recalled for Defective Sensors

    Degania Silicone is recalling 12,532 Foley catheters with temperature sensors because defective sensors may display lower body temperatures than the patient's actual temperature.

    Product
    Foley Catheter with temperature sensor 400TM 18FR, Catalogue Number 102201101880TY Product Usage: This is sterile, single use, two-way silicone Foley Catheter with a thermistor embedded in the third lumen. It is intended for use in the drainage/ collection of urine from the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1192-2018·2018-09-26

    Beaumont Bio-Med Recalls Skin Irritation Homeopathic Spray Due to CGMP Deviations

    Beaumont Bio-Med is recalling Skin Irritation & Itch Response Homeopathic Formula due to manufacturing deviations that could result in possible microbial contamination.

    Product
    Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7002-7
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3189-2018·2018-09-26

    Siemens Artis Q X-Ray Systems Recalled for Temperature Control Defect

    Siemens is recalling 429 Artis Q Interventional Fluoroscopic X-Ray Systems because a temperature control defect may cause the detector to cool down outside its designed working range.

    Product
    Artis Q Interventional Fluoroscopic X-Ray System, Model Numbers 10848280, 10848281, 10848282, 10848283, 10848354 & 10848355
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1198-2018·2018-09-26

    Beaumont Bio-Med Recalls Colds & Flu Response Homeopathic Formula

    Beaumont Bio-Med is recalling Colds & Flu Response Homeopathic Formula due to potential microbial contamination from manufacturing deviations.

    Product
    Colds & Flu Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7012-7
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1197-2018·2018-09-26

    Beaumont Bio-Med Recalls Allergy & Hay Fever Relief Homeopathic Formula

    Beaumont Bio-Med is recalling 124 bottles of Allergy & Hay Fever Relief Homeopathic Formula due to CGMP deviations that could result in possible microbial contamination.

    Product
    Allergy & Hay Fever Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7011-7
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3184-2018·2018-09-26

    Ortho-Clinical VITROS Chloride Slides Recalled for Analytical Performance Issues

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Cl- Slides because they failed to meet performance standards for urine samples.

    Product
    VITROS Chemistry Products Cl- Slides, Product Code 684 4471 Product Usage: VITROS Cl Slides (Product Code 684 4471) - For in vitro diagnostic use only. VITROS Chemistry Products Cl- Slides quantitatively measure chloride (Cl-) concentration in serum, plasma and urine using…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1214-2018·2018-09-26

    Lupin Recalls Morphine Sulfate Extended-Release Tablets Due to Impurity

    Lupin Pharmaceuticals is recalling specific lots of Morphine Sulfate Extended-Release Tablets because testing found an impurity exceeding safety limits.

    Product
    MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3193-2018·2018-09-26

    Ortho-Clinical VITROS Chemistry CREA Slides Recalled for Measurement Accuracy Issues

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry CREA Slides because they failed to meet accuracy standards for low-end creatinine measurements in serum and urine.

    Product
    VITROS Chemistry Products CREA Slides, Product Code 680 2584 Product Usage: VITROS CREA Slides (Product Code 680 2584) - For in vitro diagnostic use only. VITROS Chemistry Products CREA Slides quantitatively measure creatinine (CREA) concentration in serum, plasma, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3196-2018·2018-09-26

    Smiths Medical Recalls Mislabeled Arterial Blood Sampling Kits

    Smiths Medical ASD Inc. is recalling 29,600 Portex Pulsator Arterial Blood Sampling Kits because they were mislabeled with incorrect labels.

    Product
    Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, REF 4080P-2, Sterile, RX. The firm name on the label is Smiths Medical ASD, Inc., Keene, NH.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1212-2018·2018-09-26

    InvaGen Recalls Bupropion Hydrochloride Tablets Due to Impurity Levels

    InvaGen Pharmaceuticals is recalling specific lots of Bupropion Hydrochloride ER tablets because older batches failed impurity specifications.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V666000·2018-09-25

    Kia Recalls 2017-2018 Niro Hybrids for Fire Risk

    Kia is recalling 2017-2018 Niro hybrid vehicles because a faulty relay may overheat the rear seat, increasing the risk of a fire.

    Product
    KIA — KIA NIRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18230·2018-09-25

    Traeger Recalls Scout and Ranger Grills Due to Fire Hazard

    Traeger Grills is recalling Scout and Ranger portable wood pellet grills because grease can leak from the drip tray, posing a fire hazard.

    Product
    Scout and Ranger portable wood pellet grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V667000·2018-09-25

    Suzuki Recalls 2006 Grand Vitara for Power Steering Belt Tensioner Defect

    Suzuki is recalling 2006 Grand Vitara vehicles because a plastic component in the power steering system can deteriorate, potentially causing a loss of steering assist and increasing crash risk.

    Product
    SUZUKI — SUZUKI GRAND VITARA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V669000·2018-09-25

    Maintainer Service Mechanic Bodies Recalled for Driveshaft Interference Risk

    Maintainer is recalling 2017-2018 Service Mechanic Bodies mounted on Ford F-Series Super Duty trucks because a hydraulic pump may interfere with the front axle driveshaft, potentially causing separation and increasing crash risk.

    Product
    MAINTAINER — MAINTAINER SERVICE/MECHANICBODY FORD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V668000·2018-09-25

    Volvo Recalls VNL Trucks Due to Fuel Line Burst Risk

    Volvo is recalling 2016-2019 VNL trucks with Cummins ISX15 engines because a restricted fuel pump cooling circuit screen may cause the fuel line to burst.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E093000·2018-09-25

    Ioxus uStart Energy Storage Modules Recalled for Fire Risk

    Ioxus is recalling uStart energy storage modules because a seal defect may allow moisture entry, potentially causing electrical shorts and fire.

    Product
    ELECTRICAL SYSTEM:12V/24V/48V BATTERY recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18231·2018-09-25

    Provata Recalls Activity Trackers Due to Burn Hazard

    Provata Health is recalling about 30,000 promotional activity trackers because they can overheat and cause burns. Consumers should stop using the devices and contact the company for a free replacement.

    Product
    Provata activity trackers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18229·2018-09-25

    Desert Harvest Recalls Skin Repair Cream for Child-Resistant Closure Failure

    Desert Harvest is recalling Reléveum Skin Repair Cream because the bottles do not meet child-resistant closure requirements, posing a poisoning risk to young children.

    Product
    Desert Harvest Reléveum Skin Repair Cream
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V658000·2018-09-24

    Grand Design Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Grand Design is recalling 2019 Reflection, Imagine, and Transcend travel trailers because missing inner axle bearings may cause overheating and fire.

    Product
    GRAND DESIGN — GRAND DESIGN TRANSCEND, REFLECTION, IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V660000·2018-09-24

    Fontaine Recalls 2019 Infinity Trailers for Rear Impact Guard Defect

    Fontaine Trailer Company is recalling 2019 Infinity trailers because incorrect rear impact guards may not prevent vehicles from sliding underneath during a crash.

    Product
    FONTAINE — FONTAINE INFINITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V659000·2018-09-24

    Winnebago Recalls 2019 Horizon RVs Due to Door Latch Defect

    Winnebago is recalling 2019 Horizon vehicles because improperly adjusted door latch rods may allow the entry door to open while moving, increasing the risk of injury or a crash.

    Product
    WINNEBAGO — WINNEBAGO HORIZON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V655000·2018-09-21

    GM Recalls 2016-2018 Chevrolet Express and GMC Savana for Fire Risk

    General Motors is recalling 2016-2018 Chevrolet Express and GMC Savana vans due to a potential electrical short in the rear climate control module that could cause a headliner fire.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V657000·2018-09-21

    PACCAR Recalls Kenworth and Peterbilt Trucks Due to Fuel Line Burst Risk

    PACCAR is recalling 2017-2019 Kenworth and Peterbilt trucks equipped with Cummins ISX15 or X15 diesel engines because a restricted fuel pump cooling circuit screen may cause the fuel line to burst.

    Product
    KENWORTH — KENWORTH, PETERBILT T880, T680, W900, T800
    Category
    Vehicle
    Distribution
    Distributed nationwide