The Recall Desk

State

Missouri product recalls

73,827 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.

Which agencies issued them

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51151–51175 of 82328

  • SevereFDA (Devices)·Z-0328-2017·2016-11-16

    SentreHeart Recalls FindrWIRZ Guidewire Systems Due to Coating Defects

    SentreHeart Inc is recalling FindrWIRZ Guidewire Systems because the lubricious coating delaminated and flaked off three units in Germany.

    Product
    FindrWIRZ Guidewire System Catalog# 40-05 Cardiology: The system is intended for use in the cardiovascular system for introduction and positioning of over the-wire catheters and therapeutic devices during interventional procedures.
    Category
    Medical Device
    Distribution
    15 states
  • SevereFDA (Food)·F-0351-2017·2016-11-16

    Professional Botanicals Recalls MealPlex and Pearl Drinks for Undeclared Milk

    Professional Botanicals is recalling specific lots of MealPlex and Pearl meal drinks because they contain undeclared milk, a major food allergen.

    Product
    Professional Botanicals MealPlex (756 grams) and Veo Natural Pearl 3.0 (378 grams) Ultimate Meal Drinks in Plastic Tub Containers. Dietary Supplement.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0374-2017·2016-11-16

    Siemens SOMATOM Definition Flash CT Systems Recalled for Injury Risk

    Siemens is recalling 57 SOMATOM Definition Flash CT systems in the US due to a hardware issue that may expose users to rotating or electrical parts.

    Product
    SOMATOM Definition Flash system, x-ray, tomography, computed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0373-2017·2016-11-16

    Siemens SOMATOM Definition AS CT Systems Recalled for Injury Risk

    Siemens Medical Solutions is recalling 57 SOMATOM Definition AS CT systems due to a hardware issue that may expose users to rotating or electrical parts.

    Product
    SOMATOM Definition AS system, x-ray, tomography, computed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0325-2017·2016-11-16

    On the Border Tortilla Chips Recalled for Possible Metal Fragments

    Truco Enterprises is recalling On the Border Cafe Style Tortilla Chips due to possible metal fragments in the corn flour.

    Product
    On the Border Cafe Style Tortilla Chips 18 oz. and 28 oz. packaged in laminated polypropylene film with windows.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0378-2017·2016-11-16

    Stryker Recalls LFIT Anatomic V40 Femoral Heads Due to Taper Lock Failure

    Stryker Howmedica Osteonics is recalling specific lots of LFIT Anatomic V40 Femoral Heads because of reported taper lock failures that caused harm.

    Product
    LFIT Anatomic V40 Femoral Head, Low Friction Ion Treatment, Sterile, 36 mm, REF 6260-9-236; Modular components designed to be locked onto a femoral hip stem trunnion during surgery for total hip replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0309-2017·2016-11-16

    Ev3 Neurovascular Recalls Marathon and UltraFlow Micro Catheters

    Micro Therapeutics Inc. is recalling Marathon and UltraFlow HPC Flow Directed Micro Catheters because PTFE coating may delaminate and enter the bloodstream.

    Product
    Marathon Flow Directed Micro Catheter, UltraFlow HPC Flow Directed Micro Catheter Marathon Flow: The device is intended to access periphera and neurovasculature for the controlled selective infusion of physician-specified therapeutics agents such as embolization materials and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0390-2017·2016-11-16

    Maquet Accessory Adapter Recalled Due to Head Rest Slipping Hazard

    Maquet Medical Systems USA is recalling Accessory Adapter part number 600525A0 because a head rest mounted to the device slipped out of the mounting rail.

    Product
    Accessory Adapter Part number 600525A0 Product Usage: designed for the mounting of MAQUET accessories with the dovetail guide interface immediately before, during and after surgical interventions as well as for examination and treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0362-2017·2016-11-16

    Hospira Symbiq Infusion Pump Recall for White Screen Safety Shutdown

    Hospira is recalling Symbiq Two Channel Infusers that may display a white screen, causing the device to stop infusion and sound an alarm, which can delay or interrupt therapy.

    Product
    Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids. List number 16027. Note that Hospira retired this pump June 30, 2015. The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0391-2017·2016-11-16

    Trumpf Medical Systems Recalls Operating Room Table Tops for Cable Pinching

    Trumpf Medical Systems is recalling specific operating room table tops after identifying six incidents of pinched cables.

    Product
    OR Table, Top U26 H V, Model # 1909793; OR Table Top U26 H V U, Model # 1909794; OR Table Top U24 H V, Model # 1909796; OR Table Top U24 H V U, Model # 1909797; OR Table Top U24 H V W, Model # 1909798; OR Table Top U14 H V, Model # 1909799 Product Usage: Patient positioning…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0370-2017·2016-11-16

    Baxter Recalls Revaclear MAX Dialyzers Due to Potential Particulate Matter

    Baxter Healthcare is recalling 22,656 Revaclear MAX dialyzers because of potential particulate matter on the blood side of the device.

    Product
    GAMBRO Capillary Dialyzer, Polyflux(R) Revaclear MAX, STERILE, Product code 110634 Product Usage: The Revaclear Max dialyzer is a single use device used for treatment of chronic and acute renal failure by hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0361-2017·2016-11-16

    Hospira Symbiq Infusion Pump Recalled for White Screen Shutdown

    Hospira is recalling 10,337 Symbiq One Channel Infusers because a software issue may cause a white screen, stopping infusion and interrupting therapy.

    Product
    Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids. List number 16026. Note that Hospira retired this pump June 30, 2015. The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0377-2017·2016-11-16

    AtriClip LAA Exclusion System Recalled for Potential Component Failure

    AtriCure, Inc. is recalling 298 AtriClip LAA Exclusion Systems due to a potential component failure that could require medical intervention.

    Product
    AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product is used for the occlusion of the heart's left atrial appendage, under direct visualization, in conjunction with other open cardiac surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17033·2016-11-16

    Skidders Recalls Children's Shoes Due to Sharp Rivet Laceration Hazard

    Skidders Footwear is recalling about 5,500 children's canvas tennis shoes because sharp rivets pose a laceration hazard. Consumers should take shoes away from children and contact the company for a refund.

    Product
    Children's shoes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0423-2017·2016-11-16

    Brownwood Farms Cherry Butter Recalled for Undeclared Milk Allergen

    Brownwood Farms is recalling Cherry Butter products because they contain milk that is not declared on the label.

    Product
    Brownwood Farms America's Original Cherry Butter 12oz and 22oz glass bottles and 1 gallon. Private labels: Arbor Day Farm (Cherry Butter 12oz). Bowers Harbor Vineyards (Cherry Butter 12oz). Crossroads (10oz). Central Market (16oz).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0420-2017·2016-11-16

    Brownwood Farms Cherry Raspberry Preserves Recalled for Undeclared Milk

    Brownwood Farms is recalling Cherry Raspberry Preserves because the product contains milk that is not declared on the label.

    Product
    Brownwood Farms Cherry Raspberry Preserves 12oz glass bottles and 1 gallon.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0422-2017·2016-11-16

    Brownwood Farms Jalapeno Cherry Butter Recalled for Undeclared Milk

    Brownwood Farms is recalling Jalapeno Cherry Butter products because they contain milk that is not declared on the label.

    Product
    Brownwood Farms Jalapeno Cherry Butter 12oz and 20oz glass bottles and 1 gallon. Private labels: Kimmel Orchard & Vineyard (Jalapeno Cherry Butter 12oz). Benjamin Twiggs (Cherry Pepper Jam 10oz). Central Market (16oz).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0392-2017·2016-11-16

    Reshape Medical Recalls Integrated Dual Balloon System Due to Fluid Leak Risk

    Reshape Medical is recalling 114 units of the Integrated Dual Balloon System Gen 1 because distillation fluid may leak during inflation.

    Product
    ReShape Integrated Dual Balloon System, Gen 1, Model No. 01-0013-001, Catalog No. RSM110 product Usage: The ReShape Integrated Dual Balloon System is indicated for weight reduction when used in conjunction with diet and exercise, in obese patients with a Body Mass Index…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0387-2017·2016-11-16

    Roche COBAS INTEGRA c111 Analyzer Recall for Software Error

    Roche is recalling 139 COBAS INTEGRA c111 analyzers due to a software error that may cause erroneous test results.

    Product
    Roche COBAS INTEGRA c111 Analyzer, Chemistry (Photometric, Discrete), for clinical use Product Usage: The Roche COBAS INTEGRA c111 analyzer is an in-vitro diagnostic analyzer capable of performing clinical chemistry, specific protein and electrolyte tests. Analytes are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0421-2017·2016-11-16

    Brownwood Farms Pear Preserves Recalled for Undeclared Milk Allergen

    Brownwood Farms is recalling Pear & Cinnamon Preserves because the product contains milk that is not declared on the label.

    Product
    Brownwood Farms Pear & Cinnamon Preserves 10oz glass bottles and 1 gallon.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0425-2017·2016-11-16

    Brownwood Farms Cherry Preserves Recalled for Undeclared Milk

    Brownwood Farms is recalling Michigan Cherry Preserves because they contain milk that is not declared on the label.

    Product
    Brownwood Farms Michigan Cherry Preserves 12oz glass bottles and 1 gallon. Private labels: Art's Tavern (Cherry Preserves 12oz).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V829000·2016-11-16

    Mercedes-Benz Recalls S-Class Vehicles for Seat Belt Extender Defect

    Mercedes-Benz is recalling 672 S-Class vehicles because seat belt extenders may not retract or may break in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG S65, S65 AMG, AMG S63, S550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0414-2017·2016-11-16

    Wine Drizzle Recalled for Undeclared Milk Allergen in Parmesan Cheese

    Get Drizzled Custom Wine Drizzle, LLC is recalling White Wine & Garlic Wine Drizzle because it contains undeclared milk, a subingredient of Parmesan cheese.

    Product
    White Wine & Garlic Wine Drizzle, packaged in 5 oz and 8 oz glass bottles, www.winedrizzle.com, Higginsville, MO 64037
    Category
    Food
    Distribution
    1 state