The Recall Desk

State

Missouri product recalls

73,741 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.

These figures cover only the 8,500 recalls whose distribution notice names Missouri specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36426–36450 of 82241

  • HighFDA (Devices)·Z-2036-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Defect

    Cardinal Health is recalling specific lots of Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1594-2019·2019-07-31

    Jelly Belly Licorice Bridge Mix Recalled for Gluten Mislabeling

    Jelly Belly is recalling Licorice Bridge Mix because the packaging claims 'Gluten Free' but the ingredients list includes wheat flour.

    Product
    Jelly Belly Licorice Bridge Mix. Net Wt. 9 oz. (85g); 12 individual 3 oz. bags per caddy UPC: 071567981675 Manufactured by Jelly Belly Co., Fairfield, CA 94533
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V562000·2019-07-31

    Pierce Recalls 2019 Vehicles Due to Passenger Knee Air Bag Defect

    Pierce Manufacturing is recalling 174 specific 2019 models because the passenger-side knee air bag may not inflate properly during a crash, increasing injury risk.

    Product
    PIERCE — PIERCE IMPEL, ENFORCER, ARROW XT, DASH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2005-2019·2019-07-31

    Terumo Medical Recalls 23G Needles Due to Potential Sterility Compromise

    Terumo Medical Corporation is recalling 30,000 units of 23G x 1-inch needles (Lot 180811C) because a potential loss of package integrity may compromise the product's sterility.

    Product
    Terumo Needle, 23G x 1", Product Code NN2325R
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Food)·F-1944-2019·2019-07-31

    National Frozen Foods Recalls Great Value Chopped Spinach for Listeria Risk

    National Frozen Foods is recalling Great Value Chopped Spinach due to potential Listeria monocytogenes contamination. The product was distributed in seven states.

    Product
    Great Value Chopped Spinach, packed in poly bags, net wt. 12 oz. 12 oz. bag UPC: 0 78742 23740 4. master case UPC: 3 00 78742 23740 5. The retail 12 oz. bag label is read in parts: "*** Great Value Chopped Spinach ***INGREDIENTS: SPINACH *** DISTRIBUTED BY: Walmart…
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-2045-2019·2019-07-31

    Cardinal Health Recalls Monoject 201 Vet Pak Hypodermic Needles

    Cardinal Health 200, LLC is recalling Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the product's sterility barrier.

    Product
    Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2044-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Defect

    Cardinal Health is recalling Monoject 201 Vet Pak Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2052-2019·2019-07-31

    Cardinal Health Recalls Monoject Blunt Cannula Due to Sterility Barrier Defect

    Cardinal Health 200, LLC is recalling Monoject Blunt Cannula 22 G x 1-1/2" (Item code: 8881202389) because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2030-2019·2019-07-31

    Siemens Artis zee multi X-ray generator power supply recall

    Siemens is recalling 89 Artis zee multi units because a power supply issue may cause the X-ray generator to fail during procedures.

    Product
    Artis zee multi, Model Number 10094139
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2048-2019·2019-07-31

    Cardinal Health Recalls Monoject Blunt Cannulas Due to Sterility Barrier Defect

    Cardinal Health 200, LLC is recalling Monoject Blunt Cannulas because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2040-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Barrier Defect

    Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Standard Hypodermic Needle, 18 G x 1-1/2" Item code: 8881200078
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1523-2019·2019-07-31

    Gericare Iron Supplement Elixir Recalled for Potential Microbial Contamination

    Geritrex, LLC is recalling Gericare Iron Supplement Elixir due to cGMP deviations that may have resulted in microbial contamination.

    Product
    Gericare Iron Supplement Elixir Ferrous Sulfate, 220 mg, 16 fl oz. (473 mL), Distributed by: Geri-care Pharmaceuticals Corp. 1650 63rd Street Brooklyn, NY 11204, NDC 57896-709-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1604-2019·2019-07-31

    Flowers Foods Recalls Whole Wheat Hamburger Buns for Plastic Contamination

    Flowers Foods is recalling 4,793 packages of 100% Whole Wheat Hamburger Buns because they may contain small pieces of hard plastic.

    Product
    100% Whole Wheat Hamburger Buns sold under the brand names of: FLOWERS 8CT No UPC; GREAT VALUE UPC 78742 00800 4 & NATURES OWN 8CT UPC 72250 00398 8
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-2043-2019·2019-07-31

    Cardinal Health Recalls Monoject 201 Vet Pak Hypodermic Needles

    Cardinal Health is recalling Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the product's sterility barrier.

    Product
    Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2023-2019·2019-07-31

    Siemens AXIOM Artis dMP X-ray Generator Recall for Power Supply Issue

    Siemens is recalling 32 AXIOM Artis dMP units because a power supply tolerance issue may cause the X-ray generator to fail during procedures.

    Product
    AXIOM Artis dMP, Model Number 7555365
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2029-2019·2019-07-31

    Siemens Artis zee Ceiling Recalled for Power Supply Tolerance Issue

    Siemens Medical Solutions is recalling 428 Artis zee ceiling units due to a power supply tolerance issue that may cause generator failure and prevent X-ray production.

    Product
    Artis zee ceiling, Model Number 10094137
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2019-2019·2019-07-31

    Siemens AXIOM Artis dTA X-ray Generator Recall

    Siemens is recalling 178 AXIOM Artis dTA units due to a power supply issue that may prevent X-ray generation during procedures.

    Product
    AXIOM Artis dTA, Model Number 7008605
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2028-2019·2019-07-31

    Siemens Artis zee floor recalled for power supply tolerance issue

    Siemens Medical Solutions is recalling 170 Artis zee floor units due to a power supply tolerance issue that may cause generator failure and prevent X-ray imaging.

    Product
    Artis zee floor, Model Number 10094135
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1940-2019·2019-07-31

    Ragu Old World Style Sauce Recalled for Foreign Material

    Mizkan America is recalling 33,864 jars of Ragu Old World Style Sauce due to the presence of foreign material.

    Product
    Ragu Old World Style Sauce Traditional 66oz retail size sold in plastic jar
    Category
    Food
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-2031-2019·2019-07-31

    Siemens Artis zee Biplane Recalled for Generator Power Supply Tolerance Issue

    Siemens is recalling 268 Artis zee biplanes because a power supply tolerance issue may cause generator failure, preventing X-ray production during procedures.

    Product
    Artis zee biplane, Model Number 10094141
    Category
    Medical Device
    Distribution
    Distributed nationwide