The Recall Desk

State

Missouri product recalls

73,824 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.

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48926–48950 of 82325

  • SevereNHTSA·17V233000·2017-04-06

    Mitsubishi Recalls 2016 Outlander Models for Door Latch Defect

    Mitsubishi is recalling 35,674 2016 Outlander and Outlander Sport vehicles because door latches may not secure in high temperatures, increasing injury risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V234000·2017-04-06

    Micro Bird Recalls 2016-2017 G5 School Buses for Fuel Valve Defect

    Micro Bird is recalling 2016-2017 G5 school buses with specific propane kits because a fuel valve may short circuit, causing the engine to shut off while driving.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17126·2017-04-06

    Marin Pine Mountain Bicycles Recalled Due to Fork Failure Hazards

    Marin Mountain Bikes is recalling 2016 and 2017 Pine Mountain bicycles because the front forks can bend or break, posing fall and crash hazards.

    Product
    Pine Mountain bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1795-2017·2017-04-05

    Lipari Old Tyme Pepper Jack Mini Horn Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Pepper Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Pepper Jack Mini horn, 2/6#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1801-2017·2017-04-05

    Lipari Old Tyme Pepper Jack Cheese Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Pepper Jack Cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Pepper Jack Cheese, 12/8 oz.
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1790-2017·2017-04-05

    Lipari Foods Recalls Colby Jack Cheese for Listeria Risk

    Lipari Foods is recalling Copper wood Colby Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Copper wood Colby Jack Mini Horn, 4/6#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1802-2017·2017-04-05

    Lipari Old Tyme Hot Pepper Cheese Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Hot Pepper Cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Hot Pepper Cheese, 12/8 oz.
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1793-2017·2017-04-05

    Lipari Colby Jack Cheese Recalled for Listeria Contamination Risk

    Lipari Foods is recalling Old Tyme Colby Jack Longhorn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Colby Jack Longhorn, 2/14.5#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1798-2017·2017-04-05

    Lipari Colby Jack Mini Horn Cheese Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Colby Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Colby Jack Mini Horn, 2/6#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1777-2017·2017-04-05

    Saputo Recalls Dutchmark Smoked Gouda Cheese Due to Listeria Risk

    Saputo Cheese USA is recalling Dutchmark Smoked Gouda Cheese because it may be contaminated with Listeria monocytogenes.

    Product
    Dutchmark, Pasteurized Processed Smoked Gouda Cheese. Product case Label: 989922 Dutchmark, Net Wt 24.00.
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Food)·F-1799-2017·2017-04-05

    Lipari Old Tyme Colby Jack Cheese Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Colby Jack Cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Colby Jack Cheese, 12/8 oz.
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1791-2017·2017-04-05

    Lipari Foods Recalls Copperwood Pepper Jack Mini Horn Cheese

    Lipari Foods is recalling Copperwood Pepper Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Copperwood Pepper Jack Mini Horn, 4/6#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1794-2017·2017-04-05

    Lipari Old Tyme Colby Longhorn Cheese Recalled for Listeria Risk

    Lipari Foods is recalling specific lots of Old Tyme Colby Longhorn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Colby Longhorn, 2/15#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1797-2017·2017-04-05

    Lipari Old Tyme Swiss Cheese Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Swiss Cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Swiss Cheese, 2/8#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Devices)·Z-1417-2017·2017-04-05

    Philips HeartStart MRx Monitor/Defibrillator Recalled for Potential Failure to Deliver Therapy

    Philips is recalling HeartStart MRx Monitor/Defibrillators because they may fail to deliver therapy or monitoring when operating on a single battery.

    Product
    HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1792-2017·2017-04-05

    Lipari Old Tyme Colby Mini Horn Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Colby Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Colby Mini Horn, 2/6#
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Drugs)·D-0616-2017·2017-04-05

    Claris Recalls Metronidazole Injection Due to Sterility Concerns

    Claris Lifesciences Inc. is recalling 72,072 units of Metronidazole Injection, USP, 500 mg/100 mL, due to a potential leak that may compromise sterility.

    Product
    Metronidazole Injection, USP, 500 mg/100 mL, Rx only, Manufactured for: Claris Lifesciences Inc. North Brunswick NJ, 08902, By: Claris Injectable Ltd. Gujarat, India, NDC 36000-001-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V231000·2017-04-05

    E-One Recalls Emergency Vehicles Due to Front Suspension Ball Joint Defect

    E-One is recalling 2013-2016 Quest, Typhoon, and Cyclone II emergency vehicles because front suspension ball joints can loosen and separate, potentially causing a loss of steering control.

    Product
    E-ONE — E-ONE QUEST, TYPHOON, CYCLONE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0618-2017·2017-04-05

    Mylan Recalls Atorvastatin Calcium Tablets Due to Microbial Contamination

    Mylan Pharmaceuticals is recalling specific lots of Atorvastatin Calcium 10 mg tablets due to potential microbial contamination and elevated bioburden.

    Product
    Atorvastatin Calcium Tablets, 10 mg*, packaged in a) 90-count bottles (NDC 0378-3950-77); b) 90-count bottles (NDC 0378-3950-09); c) 500-count bottles (NDC 0378-3950-05); d) 500-count bottles (NDC 0378-3950-07), Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1497-2017·2017-04-05

    Merit Medical Recalls 7F Prelude Short Sheath Introducers Due to Detachment Risk

    Merit Medical Systems is voluntarily recalling 1,265 units of 7F Prelude Short Sheath Introducers because the sheath marker tips may detach during use.

    Product
    7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070, K15-00170, PSS-7F-4-035MT, PSS-7F-4MT. Produc Usage: The Merit Prelude¿ Short Sheath Introducer is intended to provide access and facilitate the percutaneous introduction of various devices into veins and/or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0621-2017·2017-04-05

    Mylan Recalls Atorvastatin Calcium Tablets Due to Microbial Contamination

    Mylan Pharmaceuticals is recalling Atorvastatin Calcium Tablets, 80 mg, due to potential microbial contamination and elevated bioburden.

    Product
    Atorvastatin Calcium Tablets, 80 mg*, packaged in a) 90-count bottles (NDC 0378-3953-09) and b) 500-count bottles (NDC 0378-3953-07), Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide