The Recall Desk

State

Kansas product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28826–28850 of 79543

  • ModerateFDA (Drugs)·D-0108-2021·2020-12-02

    Heritage Pharmaceuticals Recalls Felodipine Extended Release Tablets Due to Impurities

    Heritage Pharmaceuticals is recalling specific bottles of Felodipine Extended Release Tablets because routine testing found out-of-specification impurities.

    Product
    Felodipine Extended Release Tablets, USP 10 mg,100-count bottle, Rx only, Distributed by: Heritage Pharmaceuticals Inc. East Brunswick, NJ 08816 Made in India, NDC 23155-050-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0495-2021·2020-12-02

    Medtronic Cardioblate CryoFlex Surgical Ablation Probe Recall for Seal Defects

    Medtronic is recalling 15 units of the Cardioblate CryoFlex Surgical Ablation Probe due to a potential defect in the sterile barrier pouch seals.

    Product
    Cardioblate CryoFlex, Surgical Ablation Probe, Model Number 60SF7, PROBE 60SF7 CRYOFLEX 7CM 26L - is a single use, disposable cryoprobe that is designed for use with the CryoFlex Surgical Ablation System. The probe has an integrated thermocouple for monitoring temperature at its…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0107-2021·2020-12-02

    Fusion Health Immune Boost Recalled for Marketing Without FDA Approval

    Fusion Health and Vitality LLC is recalling 5,000 bottles of Immune Boost because the product was marketed with drug claims without an approved NDA or ANDA.

    Product
    Immune Boost with natural strawberry flavor, 8,000 IU, Supports a Healthy and Balanced Immune System, 60 mL bottle, Manufactured by: Fusion Health and Vitality, LLC. 1360 Union Hill Road, Suite 11B Alpharetta, GA 30004.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0476-2021·2020-12-02

    Luminex Recalls Verigene Processor SP Due to Unapproved Service Fixtures

    Luminex is recalling 2,838 Verigene Processor SP units because field service engineers used unapproved test fixtures to calibrate and verify the devices.

    Product
    Verigene Processor SP, Model Numbers 10-0000-07 and 10-0000-07R. Used with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product Usage: IVD sample processor, which utilizes a single-use disposable test consumable and a self-contained…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0487-2021·2020-12-02

    Advanced Bionics Recalls 28 Mislabelled Cochlear Implant Batteries

    Advanced Bionics is recalling 28 AB PowerCel 170 batteries due to mislabeling that may indicate incorrect battery life.

    Product
    AB PowerCel 170 (velvet black), REF: CI-5517-150, UDI: (01) 07630016833113 used to power the following devices: Na¿da CI Q90 Sound Processor (CI-5280), Na¿da CI Q70 Sound Processor (CI-5245) and Na¿da CI Q30 Sound Processor (CI-5260). For cochlear implant.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V748000·2020-12-01

    Hyundai Recalls Kona Electric and Nexo for Brake Software Defect

    Hyundai is recalling 2019-2021 Kona Electric and 2019-2020 Nexo vehicles because a software issue may reduce braking performance, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI KONA ELECTRIC, NEXO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V744000·2020-12-01

    Vac-Tron Recalls Excavator Trailers Lacking Rear Impact Guards

    Vac-Tron is recalling specific excavator trailers because they lack required rear impact guards, increasing the risk of injury if struck from behind.

    Product
    VAC-TRON — VAC-TRON LPSGT, LP 873 XDT, LP 873 SGT, LPXDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V747000·2020-12-01

    Nissan Recalls 2002-2006 Sentra Vehicles for Takata Air Bag Defect

    Nissan is recalling 2002-2006 Sentra vehicles because passenger air bag inflators may explode in a crash, posing a risk of serious injury or death.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V745000·2020-12-01

    Halcore Recalls 2020 Horton Emergency Vehicles Due to Display Failure

    Halcore is recalling 2020 Horton Type I and III emergency vehicles because a display processor may stop working, potentially delaying emergency services.

    Product
    HORTON — HORTON TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V741000·2020-11-30

    Mitsubishi Recalls 2016 Outlander Models for Parking Brake Corrosion Risk

    Mitsubishi is recalling 2016 Outlander and Outlander Sport vehicles because rust prevention coating on parking brake shafts may peel, causing corrosion and potential brake failure.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT, OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V742000·2020-11-30

    2021 Freightliner Cascadia clutch defect may cause disengagement

    Daimler Trucks North America is recalling 2021 Freightliner Cascadia trucks due to a manufacturing defect in the clutch assembly that may cause the clutch to disengage, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V740000·2020-11-30

    Triumph Rocket 3 Motorcycles Recalled for Air in Antilock Brake System

    Triumph is recalling certain 2020-2021 Rocket 3 motorcycles because air may have entered the rear brake ABS modulator during production. This can reduce braking efficiency over time, increasing stopping distance and crash risk.

    Product
    TRIUMPH — TRIUMPH ROCKET 3 R, ROCKET 3 GT, ROCKET 3 TFC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0078-2021·2020-11-25

    Hand Sanitizer Recalled for Methanol Contamination and Low Ethanol Content

    Albek De Mexico S.A. De C.V. is recalling NuuxSan hand sanitizer because it contained methanol and had lower ethanol levels than labeled.

    Product
    NuuxSan Instant ANTIBACTERIAL HAND SANITIZER, 70% Ethyl Alcohol (ethyl alcohol 70%), 8 fl oz. 237 mL bottle, Distributed by PCM North America LLC 9543 Bassonnet ST. STE 307, Houston, TX 77036, Made in Mexico, UPC 7 13620 00017 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0079-2021·2020-11-25

    Hand Sanitizer Recalled for Methanol Contamination and Low Ethanol Content

    Albek De Mexico S.A. De C.V. is recalling Modesa Instant Hand Sanitizer because it contained methanol and had lower ethanol content than labeled.

    Product
    Modesa INSTANT HAND SANITIZER with Moisturizers and Aloe Vera (ethyl alcohol 70% v/v) 8 fl oz (237 mL) bottle, Distributed by: Midwood brands, LLC 10611 Monroe RD. Mathews, NC 28105 Made in Mexico UPC 3 2251 38042 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0081-2021·2020-11-25

    Hand Sanitizer Recalled for Methanol Contamination and Low Ethanol Content

    Albek De Mexico is recalling Assured Instant Hand Sanitizer bottles because they contained methanol and had lower ethanol levels than labeled.

    Product
    Assured Instant Hand Sanitizer Vitamin E and Aloe (Ethyl Alcohol 70% v/v), 8 fl oz/ 237 mL bottle, Distributed By: Greenbrier International, Inc. 500 Volvo Parkway, Chesapeake, VA 23320. Made in Mexico, UPC 639277928597
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0097-2021·2020-11-25

    Ascent Pharmaceuticals Recalls Hydrocodone and Acetaminophen Tablets Due to Foreign Tablet

    Ascent Pharmaceuticals is recalling 9,768 bottles of Hydrocodone Bitartrate and Acetaminophen Tablets because one bottle contained a Losartan Potassium tablet.

    Product
    Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc. Central Islip, NY 11722, NDC 31722-943-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0080-2021·2020-11-25

    Assured Instant Hand Sanitizer Recalled for Methanol Contamination

    Albek De Mexico S.A. De C.V. is recalling 27,000 bottles of Assured Instant Hand Sanitizer because the product contained methanol and was below the label claim for ethanol content.

    Product
    Assured Instant Hand Sanitizer Aloe & Moisturizers (Ethyl Alcohol 70% v/v) 8 fl oz / 237 mL bottle, Distributed By: Greenbrier International, Inc. 500 Volvo Parkway, Chesapeake, VA 23320. Made in Mexico.UPC 639277928610
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V739000·2020-11-25

    Peterbilt 520 Recalled for Incorrect Brake Relay Connections

    PACCAR is recalling 2020-2021 Peterbilt 520 vehicles because incorrectly connected brake components may destabilize the vehicle during stability control events, increasing crash risk.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0082-2021·2020-11-25

    Next Advanced Antibacterial Hand Sanitizer Recalled for Methanol Contamination

    Albek De Mexico S.A. De C.V. is recalling Next Advanced Antibacterial Hand Sanitizer because it contained methanol and had lower ethanol levels than labeled.

    Product
    NEXT ADVANCED ANTIBACTERIAL HAND SANITIZER (Ethyl Alcohol 70%), 8 FL OZ (236 ML) bottle, Made in Mexico, Distributed by: Genomma Lab USA Inc., Houston, TX 77027. UPC 6 50240 05357 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0117-2021·2020-11-25

    Trader Joe's Gluten Free Battered Halibut Recalled for Undeclared Wheat and Milk

    Orca Bay Foods LLC is recalling Trader Joe's Gluten Free Battered Halibut because the retail packaging fails to declare wheat and milk allergens.

    Product
    Trader Joe's brand Gluten Free Battered Halibut, SKU 00503822. Product of USA. Frozen product is packed in plastic bag and sold in retail carton box (10 oz. box). Each master case contains 20/10 oz. boxes. RETAIL BOX'S label is read in parts: '***TRADER JOE'S BATTERED…
    Category
    Food
    Distribution
    19 states