The Recall Desk

State

Kansas product recalls

73,809 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,822
Critical
1,053
Severe
1,486
Most recent
2026-11-04

Of the 5,822 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 1,486 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41126–41150 of 79631

  • ModerateFDA (Devices)·Z-2334-2018·2018-07-11

    St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recall

    St. Jude Medical is recalling 986 Confirm Rx Insertable Cardiac Monitors because exposure to sub-freezing temperatures caused a transient battery voltage drop, resulting in an incorrect low battery indicator display.

    Product
    St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for the monitoring and diagnostic evaluation of patients who experience unexplained symptoms such as: dizziness, palpitations, chest pain, syncope, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2360-2018·2018-07-11

    Biocare Medical Recalls Vulcan Fast Red Chromogen Kit Due to Stability Issue

    Biocare Medical is recalling Vulcan Fast Red Chromogen Kit 2 because a stability issue in the buffer prevents the chromogen from developing.

    Product
    Vulcan Fast Red Chromogen Kit 2, part of an immunohistochemistry (IHC) procedure using an alkaline phosphatase (AP) detection system. Catalog numbers FR805-5L and FR805S
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-2344-2018·2018-07-11

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products PHYT Slides

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products PHYT Slides due to a potential for imprecise results in quality control and patient samples.

    Product
    VITROS Chemistry Products PHYT Slides, Catalog Number 8298671. in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2335-2018·2018-07-11

    St Jude Medical Recalls Merlin PCS Programmer Software for ICM Battery Display Error

    St Jude Medical is recalling Merlin PCS Programmer Software to address an incorrect low battery indicator on Confirm Rx ICM devices caused by supply chain temperature exposure.

    Product
    Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model 3650) is a portable, external device used to support the implanted device, and for this recall the software that resides on the programmer (software model 3330) is the method of delivery of the new…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0892-2018·2018-07-11

    Qualgen Recalls Estradiol Pellets Due to Incorrect or Missing Lot and Expiration Dates

    Qualgen, LLC is recalling Estradiol 20mg Pellets because the vials have incorrect or missing lot and expiration dates.

    Product
    ESTRADIOL 20mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-020-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0893-2018·2018-07-11

    Qualgen Recalls Testosterone Pellets Due to Incorrect Lot and Expiration Dates

    Qualgen, LLC is recalling Testosterone 200 mg Pellets because the vials have incorrect or missing lot and expiration dates.

    Product
    TESTOSTERONE 200 mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-120-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0907-2018·2018-07-11

    Equate ClearLAX Recalled for Unfiled NDC Numbers on Labeling

    Lupin Somerset is recalling Equate ClearLAX laxative bottles due to unfiled NDC numbers on the labels. This is a Class III recall with no reported health risks.

    Product
    Equate ClearLAX, Polyethylene Glycol 3350 Powder for Solution, OS Osmotic Laxative, OTC, packaged in a) 119 g bottle (NDC 49035-312-07), b) 238 g bottle (NDC 49035-312-08), Distributed by: Wal-mart Stores, Inc., Bentonville, AR 72716
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V458000·2018-07-10

    MV Agusta Recalls 2018 Motorcycles Due to Fork Axle Thread Damage

    MV Agusta is recalling 2018 Brutale 800 Dragster RC, F3 800, and F3 800 RC motorcycles because damaged fork axle threads may cause wheel clamping screw play and loss of control.

    Product
    MV AGUSTA — MV AGUSTA BRUTALE 800 DRAGSTER RC, F3 800, F3 800 RC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V457000·2018-07-10

    Mercedes-Benz Recalls 2017 AMG G65 for Reverse Speed Software Defect

    Mercedes-Benz is recalling 2017 AMG G65 vehicles because incorrect reverse speed limitation software may cause instability and rollover risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G65
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18185·2018-07-10

    Ortovox Recalls Avalanche Transceivers Due to Software Error

    Ortovox is recalling about 20,000 avalanche transceivers because a software error may prevent them from transmitting survivor location data, delaying rescue efforts.

    Product
    Avalanche transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V452000·2018-07-06

    Nissan Recalls 2007-2008 Versa Models Due to Air Bag Inflator Defect

    Nissan is recalling 2007-2008 Versa sedans and hatchbacks because the passenger air bag inflators may explode. This defect could cause metal fragments to strike occupants, resulting in serious injury or death.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V453000·2018-07-06

    BMW Recalls 2018-2019 X3 and X4 Models for Brake Caliper Defect

    BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because insufficient coating on rear brake caliper pistons may reduce braking performance.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V446000·2018-07-05

    Entegra Recalls 2019 Motorhomes for Windshield Wiper Defect

    Entegra is recalling 2019 Emblem and Vision motorhomes because windshield wiper arms may lift at highway speeds, reducing visibility and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA EMBLEM, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V449000·2018-07-05

    Jayco Recalls 2019 White Hawk Trailers Due to Ladder Screw Defect

    Jayco is recalling 2019 White Hawk recreational trailers because screws securing ladder steps may break, posing a fall risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V451000·2018-07-05

    Jayco Recalls 2018-2019 Motorhomes Due to Incorrect Cargo Capacity Label

    Jayco is recalling 2018-2019 Alante, Precept, Seneca, Redhawk, and Melbourne motorhomes because the cargo capacity label overstates limits, increasing crash risk.

    Product
    JAYCO — JAYCO PRECEPT, REDHAWK, ALANTE, SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V445000·2018-07-05

    Jayco Recalls 2019 Alante and Precept Motorhomes for Wiper Defect

    Jayco is recalling 2019 Alante and Precept motorhomes because windshield wiper arms may lift at highway speeds, reducing visibility and increasing crash risk.

    Product
    JAYCO — JAYCO PRECEPT, ALANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·18V448000·2018-07-05

    Keystone Recalls 2018-2019 Dutchmen Aerolite Trailers for Incorrect Rim Label

    Keystone RV Company is recalling 2018-2019 Dutchmen Aerolite recreational trailers because the Federal Certification Label lists the wrong rim size, which could lead to unsafe rim replacements.

    Product
    DUTCHMEN — DUTCHMEN AEROLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2301-2018·2018-07-04

    Philips OmniDiagnost X-ray System Recalled for Tilt Actuator Failure Risk

    Philips is recalling 477 OmniDiagnost Classic X-ray systems because a broken tilt actuator could cause the table to rotate uncontrollably, posing a risk of injury.

    Product
    OmniDiagnost Classic X-ray system Angiographic and Diagnostic, Product Nos. 70859, 708023, 708024, 708025
    Category
    Medical Device
    Distribution
    Distributed nationwide