The Recall Desk

State

Kansas product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31801–31825 of 79558

  • ModerateFDA (Food)·F-0894-2020·2020-04-01

    Alkamind Creamy Vanilla Organic Daily Protein Recalled for Unapproved Herbicide

    Organic By Nature, Inc. is recalling Alkamind Creamy Vanilla Organic Daily Protein because the flaxseed powder ingredient contains unapproved herbicide Haloxyfop.

    Product
    Alkamind Creamy Vanilla Organic Daily Protein; 450g Plastic Bottle; Finished Product Item # FAMVDP450G; 3 core alkaline proteins Distributed by Alkamind LLC, New York, NY 10028
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1541-2020·2020-04-01

    Siemens Dimension Vista Total Bilirubin Reagent Cartridge Recall

    Siemens Healthcare Diagnostics is recalling Dimension Vista Total Bilirubin reagent cartridges because they may produce inaccurate results for patients taking eltrombopag.

    Product
    Dimension Vista¿ Total Bilirubin Flex¿ reagent cartridge -In vitro Diagnostic for the determination of total bilirubin. SMN: 10445146 Product Usage: Dimension Vista TBIL method is an in vitro diagnostic test intended to quantitatively measure total bilirubin in human…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0896-2020·2020-04-01

    Organic By Nature Slim Natural Raw Meal Recalled for Unapproved Herbicide

    Organic By Nature is recalling Slim Natural Raw Meal due to the presence of unapproved herbicide Haloxyfop in the flaxseed powder.

    Product
    Erom, Inc. Slim Natural Raw Meal; Bulk; Finished product item # FGBPEIOS-E
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1599-2020·2020-04-01

    Siemens Atellica CH Ethyl Alcohol Assay Recalled for Calibration Bias

    Siemens Healthcare Diagnostics is recalling Atellica CH Ethyl Alcohol assays due to potential positive bias in results within the 10-day calibration interval.

    Product
    Atellica CH Ethyl Alcohol, Test Code ETOH, Siemens Material Number (SMN) 11097501, UDI 00630414596112. The product is an ethyl alcohol assay, IVD use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0902-2020·2020-04-01

    Organic By Nature Recalls RAWr! Life Superfoods Due to Unapproved Herbicide

    Organic By Nature is recalling RAWr! Life Organic Superfoods because the flaxseed powder ingredient contains an unapproved herbicide.

    Product
    RAWr! Life Organic Superfoods; Dietary Supplement; 300g Plastic Bottle (10.60 oz.); Finished Product Item # FHEEG300G Rawr! Life, Glendale, AZ 85308
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1552-2020·2020-04-01

    Quidel Triage TOX Drug Screen Control 1 Kit Recall for Chip Error

    Quidel is recalling Triage TOX Drug Screen Control 1 kits due to a programming error in the control chip that causes false failing results for AMP and mAMP tests.

    Product
    Quidel Triage TOX Drug Screen Control 1 Kit Box containing 5 Control 1 vials with 5 x 0.25 mL vials per box. Quidel Cardiovascular Inc. 9975 Summers Ridge Road San Diego, CA 92121 USA Quidel.com
    Category
    Medical Device
    Distribution
    19 states
  • ModerateFDA (Food)·F-0893-2020·2020-04-01

    Alkamind Creamy Chocolate Protein Recalled for Unapproved Herbicide

    Organic By Nature, Inc. is recalling Alkamind Creamy Chocolate Organic Daily Protein due to the presence of unapproved herbicide Haloxyfop in the flaxseed powder ingredient.

    Product
    Alkamind Creamy Chocolate Organic Daily Protein; 450g Plastic Bottle; Finished Product Item # FAMCDP450G; 3 core alkaline proteins Distributed by Alkamind LLC, New York, NY 10028
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1570-2020·2020-04-01

    Bard PowerPort Implantable Ports Recalled Due to Incorrect Catheter Barb Tip

    Bard Peripheral Vascular Inc is recalling 178 PowerPort implantable ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgery.

    Product
    1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard, With suture Plugs, (01)00801741026720; 2. PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single- Lumen Venous Catheter, REF: 1709601, Air Guard…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0899-2020·2020-04-01

    Purim Daily Fiber Blend Recalled for Unapproved Herbicide Contamination

    Organic By Nature, Inc. is recalling Purim Daily Fiber Blend because the flaxseed ingredient contains unapproved herbicide Haloxyfop.

    Product
    Purim Daily Fiber Blend - Original unflavored; 540g Plastic Bottle, 180g Plastic Bottle; Finished Product Item#: 2014, 2014-P65, 2015, 2015-P65 Purim - Rancho Dominguez, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1049-2020·2020-04-01

    FDA Recalls Colostat Homeopathic Remedy Due to Incorrect Labeling

    Grato Holdings, Inc. is recalling 659 bottles of Colostat homeopathic remedy because the indications on the product label are incorrect.

    Product
    COLOSTAT — COLOSTAT (RHAMNUS PURSHIANA, SPIGELIA ANTHELMIA, TARAXACUM OFFICINALE, CAJUPUTUM, HYDRASTIS CANADENSIS, ALUMINA, CINA, CINCHONA OFFICINALIS, LYCOPODIUM CLAVATUM, MAGNESIA PHOSPHORICA, MANDRAGORA OFFICINARUM, NUX VOMICA)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E018000·2020-03-31

    Cummins Recalls B6.7 Diesel Engines Due to Fuel Heater Fire Risk

    Cummins is recalling specific B6.7 diesel engines used in school buses, trucks, and emergency vehicles because the fuel heater may overheat, melt, or cause a fire.

    Product
    FUEL SYSTEM, DIESEL: PRE-HEATER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V189000·2020-03-31

    Subaru Recalls 2019 Crosstrek Vehicles for Rear Seat Belt Defect

    Subaru is recalling 2019 Crosstrek vehicles because the rear seat belt locking mechanism may not function as intended, increasing injury risk in crashes.

    Product
    SUBARU — SUBARU CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V188000·2020-03-30

    Nissan Recalls NV, Titan, Armada, QX56 for Air Bag Inflator Defect

    Nissan is recalling 216,678 vehicles from 2011-2017 because the driver-side air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    INFINITI — INFINITI, NISSAN QX56, NV, ARMADA, TITAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V186000·2020-03-27

    Can-Am Recalls 2020 Spyder RT Motorcycles Due to Brake Failure Risk

    Bombardier is recalling 2020 Can-Am Spyder RT motorcycles because a brake support could break during emergency braking, causing total loss of braking ability.

    Product
    CAN-AM — CAN-AM SPYDER RT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V185000·2020-03-26

    BMW Recalls 328d Vehicles for Driveline Joint Defect

    BMW is recalling 2013-2016 328d xDrive vehicles because a driveline joint may fail, causing loss of rear power and increasing crash risk.

    Product
    BMW — BMW 328D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V183000·2020-03-26

    Chrysler Recalls 2019 Jeep Grand Cherokee and Dodge Durango for Driveline Defect

    Chrysler is recalling 2019 Jeep Grand Cherokee and Dodge Durango vehicles because insufficiently hardened front differential pinion gears can wear down, leading to a loss of power or the PARK function.

    Product
    JEEP — JEEP, DODGE GRAND CHEROKEE, DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E017000·2020-03-26

    Land Rover Recalls 2020 Range Rover Evoque Headliners for Safety Defect

    Land Rover is recalling 2020 Range Rover Evoque vehicles because some headliners lack a required metal plate, potentially reducing head impact protection in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V180000·2020-03-26

    2019 Mercedes-Benz and Freightliner Sprinter Recall for Manual Error

    Daimler Vans USA is recalling 2019 Sprinter vans because the Operator's Manual may contain incorrect information about the automatic parking function, potentially increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 1500, SPRINTER 2500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V184000·2020-03-26

    GM Recalls 2019-2020 Chevrolet Bolt EV for Rear Door Cable Defect

    General Motors is recalling 2019-2020 Chevrolet Bolt EVs because a rear door cable may be too long, potentially causing the door to open unintentionally while driving.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1499-2020·2020-03-25

    Philips Recalls HeartStart MRx Defibrillators Due to Internal Damage Risk

    Philips is recalling HeartStart MRx Monitor/Defibrillators because internal damage from drops or shocks may prevent therapy delivery, even if the device appears undamaged.

    Product
    HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, and M3536M9.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0860-2020·2020-03-25

    Chicago Indoor Garden Recalls Sprout Salad Due to E. coli Outbreak

    Chicago Indoor Garden, Inc. is recalling Sprout Salad 6 oz. because FDA analysis found E. coli and linked the product to an outbreak.

    Product
    Sprout Salad 6 oz. Product contains red clover sprouts.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0861-2020·2020-03-25

    Chicago Indoor Garden Recalls Mixed Greens Contaminated with E. coli

    Chicago Indoor Garden is recalling Mixed Greens containing red clover sprouts because FDA testing found E. coli. The product was distributed nationwide, primarily through Whole Foods.

    Product
    Mixed Greens 4 oz. Product contains red clover sprouts.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0858-2020·2020-03-25

    Chicago Indoor Garden Recalls Red Clover Products Due to E. coli

    Chicago Indoor Garden, Inc. is recalling Red Clover products because FDA analysis found E. coli and linked the firm to an outbreak.

    Product
    Red Clover 4 oz, Red Clover 2 Lbs. Products have Red Clover as an ingredient.
    Category
    Food
    Distribution
    Distributed nationwide