The Recall Desk

State

Missouri product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45301–45325 of 82318

  • HighFDA (Food)·F-0336-2018·2017-11-29

    Shoreline Fruit Recalls Dark Chocolate Covered Cherries Due to Undeclared Milk

    Shoreline Fruit is voluntarily recalling dark chocolate covered cherries because the supplier recalled dark chocolate containing undeclared milk.

    Product
    Shoreline Fruit Dark Choc Covered Montmorency Cherries packaged in 25-pound corrugated box
    Category
    Food
    Distribution
    47 states
  • HighFDA (Food)·F-0401-2018·2017-11-29

    Ventura Foods Recalls SunGlow Margarine Due to Undeclared Soy Lecithin

    Ventura Foods is recalling SunGlow Unsalted European Style Butter Blend Margarine because it contains undeclared soy lecithin, a common allergen.

    Product
    SunGlow, Unsalted European Style Butter Blend Margarine (16953 SNG), Net Wt 16 oz (1 lb) 454 g. Keep Refrigerated. UPC 26700-13499. Outer case: Net Wt 36 lb (16.32 kg). UPC 1 00 26700 13499 6. Ventura Foods, Brea, CA 92821
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-0120-2018·2017-11-29

    Halyard Closed Suction System Recalled for Potential Saline Vial Leaks

    Halyard Health is recalling specific lots of Closed Suction Systems because the saline vials may leak, potentially exposing contents to infectious agents.

    Product
    Halyard Closed Suction System for Adults, 14 F, Elbow, Directional Tip, Wet Pak. 12 vials per kit, 20 kits per case.
    Category
    Medical Device
    Distribution
    38 states
  • HighCPSC·18046·2017-11-29

    Libbey Recalls Bourbon Taster Glasses Due to Laceration Hazard

    Libbey Glass is recalling approximately 229,000 Bourbon Taster Glasses because they can break during normal use, posing a laceration hazard.

    Product
    Bourbon Taster Glasses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0163-2018·2017-11-29

    Medline Plastic Transfer Belts Recalled for Locking Mechanism Failure

    Medline Industries is recalling 1,428 plastic transfer belts because the locking mechanism may fail, allowing the strap to slip through the buckle.

    Product
    Transfer/Gait Belt, Plastic, Wipeable, packaged in plastic bag, 36 plastic bags per box.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0161-2018·2017-11-29

    Zimmer Biomet Recalls ROSA Surgical Device Software

    Zimmer Biomet is recalling 29 ROSA Surgical Devices due to a software issue affecting cooperative endoscopy mode.

    Product
    ROSA Surgical Device 2.5.8 It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional imaging software, and uses fiducial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0085-2018·2017-11-29

    Lorazepam Tablets Recalled Due to Incorrect Strength Labeling

    Leading Pharma, LLC is recalling Lorazepam tablets labeled as 0.5 mg but containing 1 mg. The recall addresses a labeling error affecting 2,952 bottles nationwide.

    Product
    LORAZEPAM — LORAZEPAM (LORAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0093-2018·2017-11-29

    West-Ward Recalls Dexamethasone Sodium Phosphate Injection Due to Impurities

    West-Ward Pharmaceuticals is recalling specific lots of Dexamethasone Sodium Phosphate Injection because of high out-of-specification results for a related compound.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0094-2018·2017-11-29

    West-Ward Recalls Dexamethasone Sodium Phosphate Injection Due to Impurity

    West-Ward Pharmaceuticals is recalling Dexamethasone Sodium Phosphate Injection due to high levels of a related compound impurity.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V761000·2017-11-27

    Daimler Recalls 2008-2018 Trucks for Brake Light Switch Defect

    Daimler Trucks North America is recalling 2008-2018 Freightliner and Western Star trucks because the brake light switch may fail to activate lights after hard braking, increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 5700, 4900, 4700, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0365-2018·2017-11-22

    West Creek BBQ Sauce Recalled for Undeclared Egg

    CFS West Holdings Inc. is recalling West Creek Original BBQ Sauce because it may contain undeclared egg.

    Product
    West Creek Original BBQ Sauce, Net Contents 1 Gal, Distributed by Performance Food Group, Richmond, VA packaged in plastic jugs.
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-0367-2018·2017-11-22

    Texas Roadhouse Barbecue Sauce Recalled for Undeclared Egg

    CFS West Holdings Inc is recalling Texas Roadhouse Barbecue Sauce because it may contain undeclared egg. The product was distributed to distributors in 12 states.

    Product
    Texas Roadhouse Barbecue Sauce, NET 3/2 gallon, Mfg. exclusively for: Texas Roadhouse Restaurants, Louisville, KY, packaged in plastic pouches.
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-0363-2018·2017-11-22

    Monarch Worcestershire Sauce Recalled for Undeclared Egg

    CFS West Holdings Inc. is recalling Monarch Worcestershire Sauce because it may contain undeclared egg. The product was distributed to distributors in 12 states.

    Product
    Monarch Worcestershire Sauce, Net 1 gallon, Distributed by US Foods, Inc. Rosemont, IL, packaged in plastic jugs.
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-0364-2018·2017-11-22

    West Creek Sweet BBQ Sauce Recalled for Undeclared Egg

    CFS West Holdings Inc. is recalling West Creek Sweet BBQ Sauce because it may contain undeclared egg, a major food allergen.

    Product
    West Creek Sweet BBQ Sauce, Net Contents 1 Gal, Distributed by Performance Food Group, Richmond, VA packaged in plastic jugs.
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-0395-2018·2017-11-22

    doTERRA Recalls Slim & Sassy TrimShake for Undeclared Milk Allergen

    doTERRA is voluntarily recalling Slim & Sassy TrimShake mixes because they contain an undeclared milk allergen.

    Product
    Slim & Sassy¿ TrimShake Vanilla, SKU 35180001, 1 lb 5.9 oz, HDPE tub
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0366-2018·2017-11-22

    CFS West BBQ Sauce Recalled for Undeclared Egg

    CFS West Holdings Inc is recalling BBQ Sauce packed for Carl's Jr. and Hardee's because it may contain undeclared egg.

    Product
    BBQ Sauce, 200/0.88 oz Net Wt 11 lbs, Packed exclusively for Carl's Jr. Restaurants LLC, Hardee's Restaurants LLC, Carpinteria, CA. Packed packaged in plastic cups.
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-0394-2018·2017-11-22

    doTERRA Recalls Slim & Sassy TrimShake for Undeclared Milk Allergen

    doTERRA is voluntarily recalling Slim & Sassy TrimShake chocolate and vanilla mixes because they contain an undeclared milk allergen.

    Product
    Slim & Sassy¿ TrimShake Chocolate, SKU 35200001, 1 lb 5.9 oz, HDPE tub
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V753000·2017-11-22

    DRV Recalls RVs with Defective Kidde Fire Extinguishers

    DRV Suites is recalling specific recreational vehicles equipped with certain Kidde fire extinguishers that may clog, require excessive force to activate, or have nozzles that detach.

    Product
    DRV — DRV MOBILE SUITE, MOBILE SUITE ESTATES, SELECT, TRADITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0090-2018·2017-11-22

    WalkMed Infusion Pump Reservoir Bags Recalled for Fluid Leaks

    WalkMed, LLC is recalling 25,920 infusion pump reservoir bags due to reported fluid leaks at the luer connection.

    Product
    Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Number IPR-86/10 65 mL and Reservoir Bag for WalkMed Infusion Pump Part Number 204821 Catalog Number IPR-150/10 150 mL The WalkMed Reservoir Bag is designed for use with the WalkMed 350VL Ambulatory pump and is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0339-2018·2017-11-22

    Aurora Dark Chocolate Cherries Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Cherries in 8.5 oz cups and 11 oz tubs due to undeclared milk.

    Product
    Aurora Brand Dark Chocolate Cherries packaged in: 8.5 oz. Plastic Cup 11 oz. Square Plastic Tub
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V754000·2017-11-22

    Bison Recalls 2010 Recreational Trailers Due to Fire Extinguisher Defect

    Bison Coach is recalling 2010 Stratus, Aluma Sport, Trail Express, and Trail Hand trailers because their fire extinguishers may clog or detach, posing injury risks.

    Product
    BISON — BISON STRATUS, TRAIL HAND, ALUMA SPORT, TRAIL EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0096-2018·2017-11-22

    Zimmer Biomet ROSA Surgical Device Recalled for Potential Force Sensor Break

    Zimmer Biomet is recalling 21 ROSA Surgical Devices due to a possible break in the Force Sensor connector. The devices were distributed to facilities in Ohio, Michigan, and Texas.

    Product
    ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0348-2018·2017-11-22

    Uncle Buck's Dark Chocolate Peanuts Recalled for Undeclared Milk Allergen

    Ruckers Makin Batch Candies is recalling Uncle Buck's and Family Choice Dark Chocolate Peanuts due to undeclared milk. The voluntary recall affects 1,944 units distributed in 21 states.

    Product
    dark chocolate peanuts, 8.5 oz.
    Category
    Food
    Distribution
    21 states