The Recall Desk

State

Missouri product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39251–39275 of 82307

  • SevereFDA (Devices)·Z-0719-2019·2019-02-13

    Smiths Medical Recalls Portex Unit Dose Normal Saline Due to Sterility Concerns

    Smiths Medical is recalling Portex Unit Dose 5 ml Normal Saline because leaking containers may lack sterility assurance, posing a risk of exposure to infectious agents.

    Product
    Portex Unit Dose 5 ml Normal Saline (0.9%)¿¿¿¿ ¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0793-2019·2019-02-13

    Pizza Blends Recalls Paul Revere's Pizza Crust Mix Due to Salmonella Risk

    Pizza Blends, LLC is recalling Paul Revere's Pizza Crust Mix because an ingredient may be contaminated with Salmonella. The product was distributed to customers in 19 states and one Canadian province.

    Product
    Paul Revere's Pizza, Pizza Crust Mix, Manufactured by Pizza Blends Bellevue, WA packaged in 26.70 lb bags.
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Devices)·Z-0721-2019·2019-02-13

    Smiths Medical Recalls Portex 5ml Normal Saline Units Due to Sterility Issues

    Smiths Medical is recalling 106,000 units of Portex 5ml Normal Saline due to leaking containers that may compromise sterility and expose patients to infectious agents.

    Product
    Portex 5ml Normal Saline (0.9%) Unit Dose¿¿¿¿ ¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0717-2019·2019-02-13

    Medline Sterile Water Humidifier Recalled for Leaking Containers

    Smiths Medical is recalling Medline sterile water humidifiers because leaking containers may expose patients to infectious agents.

    Product
    Medline 300-350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0718-2019·2019-02-13

    Medline Prefilled 350 ml Sterile Solution Recall Due to Leaking

    Medex Cardio-Pulmonary Inc. is recalling 235,560 units of Medline Prefilled 350 ml Sterile Solution because leaking containers may compromise sterility and expose patients to infectious agents.

    Product
    Medline Prefilled 350 ml Sterile¿¿¿¿ ¿¿¿¿ ¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0716-2019·2019-02-13

    Smiths Medical Recalls Intermed 550 ml Sterile Water Humidifiers

    Smiths Medical is recalling Intermed 550 ml Sterile Water Humidifiers due to leaking containers that may compromise sterility and expose patients to infectious agents.

    Product
    Intermed 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0787-2019·2019-02-13

    Pizza Blends Pizza Dough Mix Recalled for Potential Salmonella Contamination

    Pizza Blends is recalling 24 lb bags of The Great American Pizza Dough Mix With Yeast because an ingredient may be contaminated with Salmonella.

    Product
    The Great American by Pizza Blends, Pizza Dough Mix With Yeast, Manufactured by Pizza Blends, Inc. San Antonio, TX. packaged in 24 lb bags.
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Devices)·Z-0720-2019·2019-02-13

    Smiths Medical Recalls Portex Normal Saline Units Due to Sterility Concerns

    Smiths Medical is recalling Portex Unit Dose 15 ml Normal Saline products because leaking containers may compromise sterility, potentially exposing patients to infectious agents.

    Product
    Portex Unit Dose 15 ml Normal Saline ¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0830-2019·2019-02-13

    HyVee Salted Caramel Bettercreme Cheesecakes Recalled for Salmonella

    Hy-Vee Stores Inc is recalling Salted Caramel Bettercreme cheesecakes because the product contained an ingredient that tested positive for Salmonella.

    Product
    HyVee brand Salted Caramel-flavored Bettercreme cheese cakes packaged in the following ways: 1) Sea Salted Caramel Bettercreme Cheesecake, Net Wt. 7 OZ, HyVee West Des Moines, IA UPC 02 82325 XXXXX packaged in clear plastic containers; 2) Sea Salted Caramel Bettercreme…
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0824-2019·2019-02-13

    Hy-Vee Cherry Cheesecakes Recalled Due to Salmonella Contamination

    Hy-Vee is recalling cherry cheesecakes because they tested positive for Salmonella. The products were sold in eight states.

    Product
    HyVee brand cherry cheese cakes packaged in the following ways: 1) Cheesecake, Net Wt. 8 OZ, HyVee West Des Moines, IA UPC 02 80142 XXXXX packaged in clear plastic containers; 2) Cheesecake Family Size, Net Wt. 32 OZ, HyVee West Des Moines, IA 02 80141 XXXXX, packaged in…
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0828-2019·2019-02-13

    Hy-Vee Oreo Bettercreme Cheesecakes Recalled for Salmonella

    Hy-Vee is recalling Oreo-flavored Bettercreme cheesecakes because the product tested positive for Salmonella. Consumers in eight states should discard the affected items.

    Product
    HyVee brand Oreo-flavored Bettercreme cheese cakes packaged in the following ways: 1) Oreo Bettercreme Cheesecake, Net Wt. 8 OZ, HyVee West Des Moines, IA UPC 02 82331 XXXXX packaged in clear plastic containers; 2) Oreo Bettercreme Cheesecake, Net Wt. 29 OZ, HyVee West Des…
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·19E012000·2019-02-13

    Dana Recalls Ultimate Dana 44 Front Axles Due to Seizing Risk

    Dana Incorporated is recalling certain Ultimate Dana 44 Front Axles because the pinion tail bearing may seize, preventing the axle from rotating and increasing crash risk.

    Product
    SUSPENSION:FRONT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0789-2019·2019-02-13

    Pizza Blends Recalls Dough Mix Due to Salmonella Risk

    Pizza Blends, LLC is recalling Very Good Foods Complete Round Dough Mix because an ingredient may be contaminated with Salmonella.

    Product
    Very Good Foods, Complete Round Dough Mix, Manufactured Exclusively for Askar Brands, Bloomfield Hills, MI, packaged in 27 lb bags.
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-0784-2019·2019-02-13

    Pizza Blends Recalls Chicago's Pizza Base Mix Due to Salmonella Risk

    Pizza Blends, LLC is recalling Chicago's Pizza Base Mix because an ingredient may be contaminated with Salmonella. The product was distributed to customers in 20 states and Ontario.

    Product
    Chicago's Pizza Base Mix, Manufactured Exclusively for Chicago's Pizza, Greenfield, IN packaged in 30 lb bags.
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-0786-2019·2019-02-13

    Pizza Blends Recalls Dough Mix Due to Potential Salmonella Contamination

    Pizza Blends, LLC is recalling specific lots of The Great American Pizza Dough Mix No Yeast because an ingredient may be contaminated with Salmonella.

    Product
    The Great American by Pizza Blends, Pizza Dough Mix No Yeast, Manufactured by Pizza Blends, Inc. San Antonio, TX. packaged in 24 lb bags.
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-0788-2019·2019-02-13

    Pizza Blends Recalls Peter Piper Pizza Dough Due to Salmonella Risk

    Pizza Blends, LLC is recalling Peter Piper, Two-N-One Dough manufactured for Peter Piper Pizza because an ingredient may be contaminated with Salmonella.

    Product
    Peter Piper, Two-N-One Dough, Manufactured Exclusively for Peter Piper Pizza, Phoenix, AZ. packaged in 26 lb bags.
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Devices)·Z-0714-2019·2019-02-13

    Smiths Medical Recalls Intermed 350 ml Sterile Water Humidifiers

    Smiths Medical is recalling Intermed 350 ml Sterile Water Humidifiers due to leaking containers that may compromise sterility and expose patients to infectious agents.

    Product
    Intermed 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ ¿¿¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0713-2019·2019-02-13

    Smiths Medical Recalls Portex Sterile Water Pour Bottles Due to Leaking

    Smiths Medical is recalling Portex 500 ml Sterile Water USP Pour Bottles because leaking containers may compromise sterility and expose users to infectious agents.

    Product
    Portex 500 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0790-2019·2019-02-13

    Pizza Blends Recalls Custom Pizza Flour Due to Salmonella Risk

    Pizza Blends, LLC is recalling 198 cases of Village Pizza & Seafood Custom Pizza Flour because an ingredient may be contaminated with Salmonella.

    Product
    Village Pizza & Seafood, Custom Pizza Flour, Manufactured Exclusively for Village Pizza & Seafood League City, TX, packaged in 21.7 lb bags.
    Category
    Food
    Distribution
    18 states
  • SevereNHTSA·19V096000·2019-02-13

    BMW Recalls 2019 X5 Models for Loose Driver's Seat Bolts

    BMW is recalling 2019 X5 xDrive40i and xDrive50i vehicles because driver's seat and seat belt bolts may not be properly tightened, increasing injury risk in a crash.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V094000·2019-02-13

    Volkswagen Recalls 2019 Beetles for Brake Warning Light Defect

    Volkswagen is recalling 2019 Beetle and Beetle Convertible vehicles because the instrument cluster may fail to display a visual warning when a brake system failure is detected.

    Product
    VOLKSWAGEN — VOLKSWAGEN BEETLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0424-2019·2019-02-13

    Mylan Recalls Dymista Nasal Spray Due to Broken Glass Risk

    Mylan Pharmaceuticals is recalling 10,390 bottles of Dymista nasal spray because the glass bottles may have broken glass in the neck area.

    Product
    DYMISTA — DYMISTA (AZELASTINE HYDROCHLORIDE AND FLUTICASONE PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0844-2019·2019-02-13

    General Mills Recalls Gold Medal Flour Due to Salmonella Risk

    General Mills is recalling Gold Medal Unbleached All Purpose Flour due to potential Salmonella contamination. Consumers should check their pantries for the specific product details.

    Product
    Gold Medal Unbleached All Purpose Flour. Net Wt 5 lb. (2.26kg). UPC 16000-19610. Distributed By General Mills Sales, Inc., Minneapolis, MN 55440 Cook Before Sneaking a Taste. Flour is Raw. Please Cook Fully Before Enjoying.
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-0801-2019·2019-02-13

    Radiometer ABL800 FLEX Recalled for Underestimated Creatinine Measurements

    Radiometer America Inc. is recalling ABL800 FLEX analyzers because creatinine measurements may be underestimated by up to 28%, potentially affecting patient safety during radiocontrast x-ray investigations.

    Product
    Product: ABL800 FLEX with Crea. The ABL800 with Crea is available in the following configurations: ABL817, ABL827 and ABL837. ABL800 Series Ref. 393-803, 393-804, 393-805, 393-806, 393-820, 393-821, 393-825, 393-826, 393-835, 393-836, 393-844, 393-845.
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Devices)·Z-0820-2019·2019-02-13

    Bone Marrow Biopsy Needle Recall Due to Sterile Seal Manufacturing Issue

    Angiotech is recalling 504 bone marrow biopsy needles due to a manufacturing issue affecting the sterile seal on blister trays.

    Product
    Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x 5 cm - Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.
    Category
    Medical Device
    Distribution
    Distributed nationwide