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.

Which agencies issued them

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.

36376–36400 of 82241

  • SevereFDA (Drugs)·D-1527-2019·2019-07-31

    Geritrex Recalls Preferred Plus Dioctyl Liquid Stool Softener Due to Microbial Contamination

    Geritrex, LLC is recalling Preferred Plus Dioctyl Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.

    Product
    Preferred Plus Dioctyl Liquid Stool Softener (Docusate Sodium), 50mg/5mL, 16 FL. Oz. (1 PT.) 473 mL, Manufactured by RIJ Pharmaceutical Corp. 40 Commercial Avenue Middletown, NY 10941, Distributed by Kinray Inc. Whitestone, NY 11357, NDC 53807-216-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1498-2019·2019-07-31

    Pharma-Natural Recalls Double Tussin DM Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling 500 bottles of Double Tussin DM because the product was manufactured with current good manufacturing practice violations.

    Product
    DOUBLE TUSSIN DM (Dextromethorphan Hbr 20 mg, Guaifenesin 300 mg) in each 5ml teaspoon, 4 FL OZ (120 mL) bottle, Distributed by: Pamby Dist., Miami, FL 33414, NDC 63708-121-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1526-2019·2019-07-31

    Gericare Geri-Tussin DM Recalled for Potential Microbial Contamination

    Geritrex, LLC is recalling Gericare Geri-Tussin DM due to cGMP deviations that may result in microbial contamination.

    Product
    Gericare Geri-Tussin DM, 16 FL OZ (473 mL), Geri-care Phamaceuticals Corp. 1650 63rd Street Brooklyn, NY, NDC 57896-660-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1520-2019·2019-07-31

    Geritrex Recalls Diphenhydramine Oral Liquid Due to Potential Microbial Contamination

    Geritrex, LLC is recalling 8,645 bottles of Diphenhydramine Oral Liquid due to cGMP deviations that may result in microbial contamination.

    Product
    Diphenhydramine Oral Liquid Alcohol Free, 12.5 mg/5 mL, 4 fl oz (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941, NDC 53807-204-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1965-2019·2019-07-31

    Probar Meal Superfood Slam Bars Recalled for Undeclared Milk and Soy

    Probar LLC is recalling 2,908 Superfood Slam meal bars nationwide and in Canada due to undeclared milk and soy allergens.

    Product
    PROBAR MEAL Superfood Slam, Net Wt. 3oz.(85g), Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1969-2019·2019-07-31

    Probar Chocolate Coconut Bars Recalled for Undeclared Milk and Soy

    Probar LLC is recalling 2,016 Chocolate Coconut bars because they may contain undeclared milk and soy allergens.

    Product
    PROBAR The Simply Real Bar: Chocolate Coconut, Net Wt. 85g, Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1582-2019·2019-07-31

    Brand Castle Recalls Grinch Sugar Cookie Mix Due to E. coli Risk

    Brand Castle LLC is recalling The Grinch Sugar Cookie Mix with Sprinkles because a supplier reported potential E. coli contamination in the flour used.

    Product
    The Grinch Sugar Cookie Mix with Sprinkles, 22.3 oz glass jar, 6/case
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2011-2019·2019-07-31

    Philips BrightView XCT Medical Device Recalled for Handcontroller Motion Defect

    Philips Medical Systems is recalling 427 BrightView XCT devices because a handcontroller issue may cause uncommanded motions or continued motion after buttons are released.

    Product
    BrightView XCT , Model Number 882482
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2026-2019·2019-07-31

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

    Siemens is recalling one AXIOM Artis TC unit due to a power supply tolerance issue that may cause X-ray generation failure during procedures.

    Product
    AXIOM Artis TC, Model Number 7728350
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2080-2019·2019-07-31

    Bard Nautilus Delta Port Kits Recalled for ECG Signal Loss

    Bard Peripheral Vascular is recalling specific Nautilus Delta Port Kits due to a risk of losing the intravascular ECG signal during placement procedures.

    Product
    POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 6F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; POWERPORT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2039-2019·2019-07-31

    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, 16 G x 1-1/2" Item code:8881200045
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2025-2019·2019-07-31

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

    Siemens is recalling 19 AXIOM Artis dFC units because a power supply tolerance issue may cause generator failure, preventing X-ray procedures.

    Product
    AXIOM Artis dFC, Model Number 7727717
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19E052000·2019-07-31

    Vitro Recalls Aftermarket Rear Window Glass for Non-Compliant Fragment Size

    Vitro is recalling 47,366 aftermarket rear window glass units for various vehicles because improper tempering may result in large fragments that increase injury risk in a crash.

    Product
    VISIBILITY:GLASS, SIDE/REAR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2035-2019·2019-07-31

    Spacelabs Smart Disclosure System Recalled for Patient Data Mismatch

    Spacelabs Healthcare is recalling the Smart Disclosure System because patient records were printed with waveforms from other patients.

    Product
    Spacelabs Healthcare Smart Disclosure System, Model 92810, a component of the Intesys Clinical Suite (ICS) G2.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19E053000·2019-07-31

    Mekra Lang Recalls Truck Mirror Housings Due to Detaching Glass Risk

    Mekra Lang is recalling certain Main Mirror Housings for truck cabs because improper adhesive bonding may cause the mirror glass to detach, reducing driver visibility.

    Product
    VISIBILITY:GLASS, SIDE/REAR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1605-2019·2019-07-31

    Flowers Foods Recalls Hot Dog Buns Due to Potential Plastic Contamination

    Flowers Foods is recalling 46,122 packages of hot dog buns sold under multiple brands because they may contain small pieces of hard plastic.

    Product
    Hot Dog Buns sold under the brand names of: CLOVER VALLEY 8CT UPC 70210 00760 1; FAMILY STYLE 8CT UPC 70210 01297 1; FLOWERS RESTAURANT 12CT UPC 70210 00640 6, UPC 70210 00649 9 & UPC 70210 00964 3; FOOD DEPOT 8CT UPC 72250 02439 6; GREAT VALUE 8CT UPC 78742 09728 2; IDEAL 8CT…
    Category
    Food
    Distribution
    18 states
  • HighNHTSA·19V564000·2019-07-31

    Hino Recalls 2020 NJ8J, NE8J, and NV8J Trucks for Mirror Glass Defect

    Hino is recalling 1,531 model-year 2020 NJ8J, NE8J, and NV8J trucks because exterior mirror glass may detach, reducing driver visibility and increasing crash risk.

    Product
    HINO — HINO NJ8J, NE8J, NV8J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2002-2019·2019-07-31

    Terumo Sur-vet Needle Recall Due to Potential Loss of Package Integrity

    Terumo Medical Corporation is recalling 844,000 Sur-vet Needles because a loss of package integrity may compromise the sterility of the product.

    Product
    Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Devices)·Z-2042-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Concerns

    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, 20 G x 1-1/2" bulk Item code: 8881200664
    Category
    Medical Device
    Distribution
    Distributed nationwide