The Recall Desk

State

Missouri product recalls

73,598 recalls have nationwide distribution and so reach Missouri. 8,496 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,496
Critical
1,339
Severe
2,203
Most recent
2026-10-14

Of the 8,496 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 8,496 recalls whose distribution notice names Missouri specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28601–28625 of 82094

  • HighFDA (Devices)·Z-0952-2021·2021-02-10

    Topcon Harmony Referral System Recalled for Patient Data Mixing

    Topcon Medical Systems is recalling 13 Harmony Referral System units because software flaws allowed non-unique patient IDs to merge distinct patient records and images.

    Product
    Harmony Referral System (aka Harmony RS)/ Medical Device Data System - Product Usage: intended to be used by trained healthcare professionals and clinicians to access archived multimedia data, forms and patient information.
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Food)·F-0256-2021·2021-02-10

    Champlain Chocolate Company Recalls Milk Chocolate Bars for Plastic Contamination

    Champlain Chocolate Company is recalling specific lots of Milk Chocolate Bar Library because they may contain plastic pieces.

    Product
    Lake Champlain chocolates - Milk Chocolate Bar Library 1.1 lbs.- online stock code 1Y515-000001-1; UPC: 76993385757
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0947-2021·2021-02-10

    Philips EPIQ Ultrasound Systems Recalled for Control Panel Failure Risk

    Philips is recalling 12,080 EPIQ Diagnostic Ultrasound Systems because the control panel arm assembly may break off if subjected to undue force.

    Product
    Philips EPIQ Diagnostic Ultrasound System, Models EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx & EPIQ CVxi - Product Usage: the systems can assist the interventionist and surgeon with image guidance during treatment of cardiovascular disease in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0934-2021·2021-02-10

    Brainreader Recalls Neuroreader Software Due to Database Discrepancy

    Brainreader ApS is recalling Neuroreader Medical Image Processing Software Version 2.4 because it was distributed with a reference database different from the FDA-cleared version.

    Product
    Neuroreader Medical Image Processing Software - Product Usage: intended to automate the current manual process of identifying, labeling, and quantifying the volume of segmentable brain structures identified on MR images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0245-2021·2021-02-10

    Lake Champlain Chocolates Recalls Gift Baskets for Plastic Contamination

    Champlain Chocolate Company is recalling Lake Champlain Chocolates gift baskets because they may contain plastic pieces.

    Product
    Lake Champlain Chocolates - gift basket- BE MINE; Net Wt. 2lbs.; UPC: 76993305237 Gift basket contains the following items: 21 piece Grand Valentine Chocolate Heart Assortment " 1 3oz Organic 57% Dark Chocolate Bar " 1 3 oz Raspberries and Dark Chocolate Bar " 1 1.9oz…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0948-2021·2021-02-10

    Allergan Recalls Refresh Contacts Comfort Drops Due to Missing Instructions

    Allergan PLC is recalling Refresh Contacts Contact Lens Comfort Drops because the packages are missing the Instruction For Use insert. Consumers should stop using the product and contact the manufacturer.

    Product
    REFRESH CONTACTS¿ Contact Lens Comfort Drops 0.4 fl oz (12 mL) Sterile
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0933-2021·2021-02-10

    Smith & Nephew Recalls Versabond AB Bone Cement Due to Heat Exposure

    Smith & Nephew is recalling 5,190 units of Versabond AB bone cement due to potential heat and humidity exposure that altered the product's consistency.

    Product
    VERSABOND AB 40 GRAMS FORMULATION 2, antibiotic infused bone cement, Product Number: 71271440 - Product Usage: VERSABOND is a medium viscosity bone cement which can be used for hip, knee, and shoulder implant fixation. VERSABOND AB includes the antibiotic- gentamycin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0247-2021·2021-02-10

    Chocolates of Vermont Recalled for Potential Plastic Contamination

    Champlain Chocolate Company is recalling specific lots of Chocolates of Vermont products because they may contain plastic pieces.

    Product
    Chocolates of Vermont 1.Lake Champlain Chocolates - Chocolates of Vermont - Assorted Bulk 2.5 lbs. - Online Stock code: 1Y302-000000-1 UPC: 76993305399 2. Lake Champlain Chocolates - Chocolates of Vermont - 4 Piece Sampler - 1.9 oz.- Online Stock Code -1Y302-004001-1…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0942-2021·2021-02-10

    Fresenius Medical Care Recalls NaturaLyte Liquid Acid Concentrate Due to Missing Labels

    Fresenius Medical Care is recalling 2,280 cases of NaturaLyte Liquid Acid concentrate because bottles are missing product labels.

    Product
    Fresenius Medical Care NaturaLyte Liquid Acid concentrate-Liquid Acid Concentrate for Bicarbonate Hemodialyis Part Number: 08-3251-9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0247-2021·2021-02-10

    Lupin Recalls Oseltamivir Phosphate Oral Suspension Due to Impurity Issues

    Lupin Pharmaceuticals is recalling 46,479 bottles of Oseltamivir Phosphate oral suspension because out-of-specification test results were found for Impurity C during stability testing.

    Product
    OSELTAMIVIR PHOSPHATE — OSELTAMIVIR PHOSPHATE (OSELTAMIVIR PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V060000·2021-02-08

    BMW Recalls Motorcycles for Fuel Pump Leak Fire Risk

    BMW is recalling 2011-2014 motorcycles because the fuel pump may crack and leak fuel, creating a fire risk.

    Product
    BMW — BMW K 1600 GT, R 1200 GS, K 1600 GTL, S 1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V061000·2021-02-08

    2021 PJ Trailers C5, C4, U8, and other models recalled for missing axle bearings

    Certain 2021 PJ Trailers models (C5, C4, U8, UL, U6, UC) are recalled because their suspension axles may have missing inner bearings that could cause wheel separation and increase crash risk.

    Product
    PJ TRAILERS — PJ TRAILERS U6, C4, UL, C5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·21V050000·2021-02-05

    GM Recalls Trucks and SUVs for Airbag Inflator Explosion Risk

    General Motors is recalling specific 2007-2011 trucks and SUVs because the front passenger airbag inflators may explode due to humidity, posing a risk of serious injury or death.

    Product
    GMC — GMC, CHEVROLET, CADILLAC SIERRA 3500, YUKON, TAHOE, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·21V051000·2021-02-05

    GM Recalls 2012 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling 2012 Chevrolet, GMC, and Cadillac vehicles because the front passenger airbag inflators may explode, posing a risk of serious injury or death.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SILVERADO 1500, SILVERADO 3500, YUKON, ESCALADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·21V053000·2021-02-05

    GM Recalls 2009-2013 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling specific 2009-2013 Chevrolet, GMC, and Cadillac vehicles because the front passenger airbag inflator may explode, sending metal fragments into the cabin.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC TAHOE, YUKON XL, SIERRA 1500, ESCALADE ESV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V057000·2021-02-05

    Mercedes-Benz Recalls GLE and GLS Models for Dashboard Defect

    Mercedes-Benz is recalling 2020-2021 GLE and GLS models because the dashboard may not be properly secured, which could impair airbag inflation in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450, GLE 350, GLS 450, AMG GLE53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V052000·2021-02-05

    GM Recalls 2007-2009 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling specific 2007-2009 Chevrolet, Cadillac, and GMC vehicles because the front passenger airbag inflators may explode, posing a risk of serious injury or death.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, GMC SUBURBAN, ESCALADE ESV, ESCALADE EXT, AVALANCHE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V054000·2021-02-05

    GM Recalls 2010-2014 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling specific 2010-2014 Cadillac, Chevrolet, and GMC vehicles because the front passenger airbag inflators may explode due to propellant degradation.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE EXT, SUBURBAN, TAHOE, SIERRA 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V055000·2021-02-05

    Mercedes-Benz Metris and Sprinter Recall for eCall Software Defect

    Daimler Vans USA is recalling 2016-2020 Metris and 2019-2020 Sprinter vans because the eCall system may send emergency responders to the wrong location after a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS, SPRINTER 1500, SPRINTER 2500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V058000·2021-02-05

    Mercedes-Benz vehicles recall: eCall software may fail to report correct crash location

    Mercedes-Benz is recalling 2016-2021 vehicles with eCall software that may fail to communicate the correct crash location to emergency services, potentially delaying emergency response.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH AMG GLE43, AMG GLE63, AMG GLS63, AMG E43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V056000·2021-02-05

    Mercedes-Benz Recalls 2020 GLE Models for Reverse Light Malfunction

    Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because a lighting control unit malfunction may leave the left reverse light on in other gears, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V049000·2021-02-04

    Jayco Eagle Fifth Wheel Recall for Incorrect Spring Hanger

    Jayco is recalling 2021 Eagle fifth wheel vehicles equipped with incorrect spring hangers that reduce tire clearance, increasing the risk of tire blowouts.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide