The Recall Desk

State

Kansas product recalls

73,827 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.

These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50451–50475 of 79649

  • ModerateFDA (Devices)·Z-2911-2016·2016-10-12

    Arrow Recalls Walrus Arterial Embolectomy Catheters Due to Labeling Errors

    Arrow International Inc is recalling 2,425 Walrus Arterial Embolectomy Catheters nationwide due to incorrect labeling.

    Product
    Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is intended for use in removing arterial emboli.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0020-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color Impulse Violet Due to Packaging Leaks

    Ivoclar Vivadent is recalling 25 units of Zenostar MT Color Impulse violet dental porcelain coloring due to packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color Impulse violet, art. no. 681166 Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0025-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color A4 Dental Porcelain Liquid

    Ivoclar Vivadent is recalling 11 units of Zenostar MT Color A4 dental porcelain liquid due to potential packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color A4 60ml, art. no. 681054. Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0007-2017·2016-10-12

    Sun Pharmaceutical Recalls Bupropion Hydrochloride Tablets for Dissolution Failures

    Sun Pharmaceutical Industries is recalling 31,762 bottles of Bupropion Hydrochloride Extended-Release Tablets because they failed dissolution specifications.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0009-2017·2016-10-12

    Philips Brilliance 64 CT Scanner Recalled for Infant Head Image Quality Issues

    Philips Medical Systems is recalling 185 Brilliance 64 CT scanners because infant head scans in High Resolution mode may show degraded image quality.

    Product
    Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0019-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color Impulse Grey Dental Porcelain

    Ivoclar Vivadent is recalling 60 units of Zenostar MT Color Impulse grey dental porcelain due to packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color Impulse grey, art. no. 681167 Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0001-2017·2016-10-12

    Varithena Administration Packs Recalled Due to Incorrect Syringe Type

    Biocompatibles is recalling Varithena administration packs because they contain the incorrect type of syringe. The recall covers 3,254 packs distributed nationwide.

    Product
    VARITHENA — VARITHENA (POLIDOCANOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0001-2017·2016-10-12

    Terumo CDI H/S Cuvette Recall Due to Connection Error

    Terumo is recalling CDI H/S Cuvettes because they may fail to connect to the probe, causing the monitor to display an error and preventing blood parameter display.

    Product
    CDI¿ H/S Cuvette The intended use for the CDI¿ H IS Cuvette is as follows: The CDI¿ H/S Cuvettes are intended for use with a CDI monitor during cardiopulmonary bypass procedures when continuous monitoring of blood hematocrit and oxygen saturation is desired.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2912-2016·2016-10-12

    Siemens RAPIDPoint 400 Cartridges Recalled for Chloride Calibration Error

    Siemens is recalling RAPIDPoint 400 Measurement Cartridges because of an error in the value assignment for Chloride calibrators.

    Product
    Siemens RAPIDPoint 400 Measurement Cartridge Siemens SMN numbers:10329756, 10341161
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2913-2016·2016-10-12

    Siemens RAPIDPoint 405 Cartridges Recalled for Chloride Calibration Error

    Siemens Healthcare Diagnostics is recalling RAPIDPoint 405 Measurement Cartridges due to an error in the value assignment for Chloride calibrators.

    Product
    Siemens RAPIDPoint 405 Measurement Cartridge Siemens SMN numbers: 10844812, 1028322, 10313971 , 10310469
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0006-2017·2016-10-12

    Shire Recalls Vyvanse Capsules Due to Presence of Foreign Tablets

    Shire is recalling 7,680 bottles of Vyvanse 30 mg capsules because foreign tablets or capsules were found in the product.

    Product
    VYVANSE — VYVANSE (LISDEXAMFETAMINE DIMESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V726000·2016-10-11

    Hyundai Recalls Sonata Models Due to Sunroof Detachment Risk

    Hyundai is recalling 2015-2016 Sonata and Sonata Hybrid vehicles because the panoramic sunroof panel may detach while driving, creating a road hazard.

    Product
    HYUNDAI — HYUNDAI SONATA, SONATA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V724000·2016-10-11

    Nissan Recalls 2017 Versa Vehicles for Side Air Bag Defect

    Nissan is recalling 2017 Versa vehicles because a seam in the side curtain air bags may tear during deployment, increasing the risk of injury in a crash.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V725000·2016-10-11

    Honda Recalls 2016 Civic Vehicles Due to Electric Parking Brake Defect

    Honda is recalling 2016 Civic vehicles because the electric parking brake may fail to engage immediately after the ignition is turned off, increasing the risk of the vehicle rolling away.

    Product
    HONDA — HONDA CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·091-2016 EXP·2016-10-07

    Silver Springs Farms Recalls Beef Products Due To Possible E. Coli O157:H7

    Silver Springs Farms is recalling ground beef and sandwich steak products that may be adulterated with E. coli O157:H7.

    Product
    Silver Springs Farms, Inc. Recalls Beef Products Due To Possible E. Coli O157:H7 Adulteration
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V718000·2016-10-07

    REV Recalls 2016-2017 Ambulances Due to Defective Attendant Seat Tracks

    REV Ambulance Group is recalling 39 ambulances from 2016-2017 because defective seat tracks may allow attendant seats to move rapidly during a crash, increasing injury risk.

    Product
    FRONTLINE — FRONTLINE, WHEELED COACH, MCCOY MILLER TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V721000·2016-10-07

    Newmar Recalls 2015 Dutch Star Motorhomes Due to Brake Signal Defect

    Newmar is recalling 2015 Dutch Star motorhomes because the brake signal to towed devices may not deactivate, causing dragging brakes, overheating, fire, or crashes.

    Product
    NEWMAR — NEWMAR DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V722000·2016-10-07

    Hyundai Recalls Genesis Coupe Due to Air Bag Sensor Connector Issue

    Hyundai is recalling 2010-2016 Genesis Coupe vehicles because the front passenger air bag sensor connector may dislodge, potentially causing incorrect air bag deployment in a crash.

    Product
    HYUNDAI — HYUNDAI GENESIS COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V723000·2016-10-07

    Autocar Recalls Xspotter and Xpert Vehicles for Steering Linkage Defect

    Autocar is recalling 1,132 model year 2015-2017 Xspotter and Xpert vehicles because improperly tightened steering linkage nuts could cause loss of steering.

    Product
    AUTOCAR — AUTOCAR XSPOTTER, XPERT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V719000·2016-10-07

    Winnebago Recalls 2016-2017 Travel Trailers Due to Incorrect Weight Labels

    Winnebago is recalling 2016-2017 travel trailers because weight labels list fresh water capacity in gallons instead of pounds, which may cause overloading.

    Product
    WINNEBAGO — WINNEBAGO WINNIE DROP, SPYDER, MINNIE PLUS, MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17007·2016-10-06

    Summer Infant Recalls Bath Tubs Due to Sling Detachment Risk

    Summer Infant is recalling Lil' Luxuries infant bath tubs because the fabric slings can detach, posing risks of impact injury and drowning.

    Product
    Lil' Luxuries infant bath tubs with fabric slings
    Category
    Consumer Product
    Distribution
    Distributed nationwide