The Recall Desk

State

Kansas product recalls

73,741 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,821
Critical
1,053
Severe
1,485
Most recent
2026-10-28

Of the 5,821 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,485 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38751–38775 of 79562

  • HighFDA (Food)·F-0625-2019·2018-11-28

    Cadence Gourmet Recalls Roasted Vegetable Blend for Potential Pathogen Contamination

    Cadence Gourmet LLC is recalling Roasted Vegetable Blend due to potential Salmonella and Listeria contamination from McCain Foods USA ingredients.

    Product
    Roasted Vegetable Blend; Net Weight: 30 lbs. (12 x 2.5 lb. bags) Corner Bakery Caf¿ Brand Ingredients: Zucchini, artichoke (water, citric acid and calcium chloride). Tomatoes, olive oil, canola oil, garlic, vinegar (potassium metabisulfite), salt, black pepper, spices.…
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0489-2019·2018-11-28

    Merck Minicon Clinical Sample Concentrators Recalled for Performance Issues

    Merck Millipore is recalling Minicon Clinical Sample Concentrators because they may take up to 24 hours to concentrate samples, delaying diagnostic tests.

    Product
    Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon CS-15) Minicon concentrators are non-sterile, disposable, multiwall ultrafiltration devices. Minicon¿ clinical sample concentrators are for in vitro diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0476-2019·2018-11-28

    Ortho-Clinical VITROS dLDL Reagent Recalled for Negatively Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products dLDL Reagent GENs 26 and 27 because the in vitro diagnostic may produce negatively biased results.

    Product
    VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Diagnostic to quantitatively measure LDL Cholesterol (LDLC) Product Code: 6801728 UDI (10758750006793)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0283-2019·2018-11-28

    Dr. Reddy's Recalls Clopidogrel Tablets Due to Dissolution Failure

    Dr. Reddy's Laboratories is recalling specific lots of Clopidogrel Bisulfate tablets because they failed dissolution testing during stability checks.

    Product
    CLOPIDOGREL BISULFATE — CLOPIDOGREL BISULFATE (CLOPIDOGREL BISULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0275-2019·2018-11-28

    Ecolab Recalls Medi-Stat Foam Hand Soap Due to Labeling Error

    Ecolab Inc is recalling 14,108 bottles of Medi-Stat Foam Antimicrobial Hand Soap because the label may not match the formula in the bottle.

    Product
    Medi-Stat Foam, Antimicrobial Hand Soap, Chloroxylenol 0.5%, 1250 mL (42.3 fl oz), OTC, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102, NDC 47593-503-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0388-2019·2018-11-28

    GE Healthcare Recalls DeltaVision OMX SR Imaging Systems Due to Interlock Defect

    GE Healthcare Biosciences is recalling 39 DeltaVision OMX SR Imaging Systems because the safety interlocks are not wired to be single-fault tolerant.

    Product
    DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision OMX SR Imaging System is a piece of laboratory equipment for super resolution imaging offluorescently-la beling biological samples. Techniques such as 3D Structured Illumination, Total Internal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0273-2019·2018-11-28

    Nitrofurantoin Capsules Recalled for Potential Cross-Contamination with Unrelated Ingredients

    American Health Packaging is recalling specific lots of Nitrofurantoin Capsules due to potential cross-contamination with unrelated active ingredients.

    Product
    Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals), 100 mg, 100-count Unit Dose Blisters, Rx only, Amerisource Health Services DBA American Health Packaging, 2550-A John Glenn Avenue Columbus, OH 43217, NDC 68084-446-01 (Individual Dose NDC: 68064-446-11)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V836000·2018-11-27

    Audi Recalls A5 and A4 Allroad for Passenger Air Bag Defect

    Volkswagen Group of America is recalling 2018 Audi A5 Sportback and 2017-2018 Audi A4 Allroad vehicles because a passenger air bag mounting screw may not be sufficiently tightened.

    Product
    AUDI — AUDI A5, A4 ALLROAD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V839000·2018-11-27

    Mercedes-Benz Recalls 2019 Models for Seat Belt Pre-Tensioner Defect

    Mercedes-Benz is recalling 4,969 2019 vehicles because seat belt pre-tensioners may not activate in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH E 450, S 450, C 300, S 560 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V840000·2018-11-27

    Mercedes-Benz Recalls 2019 GLC 300 for Steering Assist Failure

    Mercedes-Benz is recalling 2019 GLC 300 vehicles because a steering sensor may fail, deactivating power assist and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V833000·2018-11-27

    Lamborghini Recalls Gallardo Vehicles Due to Software Warning Failure

    Lamborghini is recalling 2011-2014 Gallardo vehicles because engine software may erase trouble codes, preventing warning lamps from illuminating for safety system failures.

    Product
    LAMBORGHINI — LAMBORGHINI GALLARDO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E107000·2018-11-27

    Wanda Recalls Aftermarket Windshields for 2014-2018 Toyota Highlanders

    Fujian Wanda is recalling aftermarket replacement windshields for 2014-2018 Toyota Highlanders because water leaks into the wire harness, potentially damaging the Engine Control Module and causing the engine to stall.

    Product
    TOYOTA — TOYOTA HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V838000·2018-11-27

    Mercedes-Benz Recalls 2018-2019 Models for Passenger Air Bag Display Error

    Mercedes-Benz is recalling specific 2018-2019 C-Class and GLC-Class vehicles because the passenger air bag status may display incorrectly, potentially leaving occupants unaware the air bag is off.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C 300, AMG GLC63S, C 350 E, C 300 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V832000·2018-11-26

    Airstream Recalls 2019 Interstate Motorhomes Due to Fuse Defect

    Airstream is recalling 2019 Interstate motorhomes because incorrect fuses may allow battery cables to overheat, increasing fire risk.

    Product
    AIRSTREAM — AIRSTREAM INTERSTATE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V830000·2018-11-26

    BMW Recalls One 2019 F850GS Motorcycle for Engine Defect

    BMW is recalling one 2019 F850GS motorcycle because engine connecting rods may be loose, risking engine damage and loss of power.

    Product
    BMW — BMW F850GS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V831000·2018-11-26

    Maserati Recalls 2014-2015 Models for Fuel Line Fire Risk

    Maserati is recalling 2014-2015 Quattroporte and Ghibli vehicles because damaged fuel lines may leak, increasing the risk of a fire.

    Product
    MASERATI — MASERATI QUATTROPORTE, GHIBLI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V824000·2018-11-26

    Volkswagen Recalls 2018-2019 Models for Missing Ignition Key Warning

    Volkswagen is recalling 2018-2019 Atlas, Tiguan, and Jetta vehicles because the instrument cluster may fail to provide an audible warning when the key is left in the ignition.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN, JETTA, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide