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.

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.

40751–40775 of 79631

  • ModerateFDA (Devices)·Z-2581-2018·2018-08-08

    GE Healthcare Recalls CT Systems with Potential Electrical Wiring Defect

    GE Healthcare is recalling 42 Discovery RT CT systems nationwide due to a potential wiring defect in the electrical panel that may affect the uninterruptible power supply.

    Product
    Discovery RT labeled as: a. MID BJG; b. HVY BJG
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2588-2018·2018-08-08

    bioMerieux Recalls VIDAS LH Test Kits Due to Calibration Issues

    bioMerieux, Inc. is recalling VIDAS LH test kits because internal tests confirmed a decrease in strip signal over time, leading to invalid calibration results.

    Product
    VIDAS LH, Reference Numbers 30406 and 30406-01. Poduct Usage: VIDAS LH is an automated quantitative test for use on the VIDAS family instruments for the determination of human luteinizing hormone in human serum or plasma (lithium heparin), using the ELFA technique (Enzyme…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2567-2018·2018-08-08

    Howmedica Custom Implant System Recalled for Missing Instructions

    Howmedica is recalling five custom implant systems because they lacked updated instructions clarifying the locking mechanism and screw warnings.

    Product
    Custom Made Implant System with Minimum Invasive Grower (MIG) component
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-1033-2018·2018-08-08

    Renaissance Lakewood Recalls Fluconazole Injection Bags for Out-of-Specification Levels

    Renaissance Lakewood, LLC is recalling 12,088 bags of Fluconazole Injection because the lots are out of specification for elevated sodium chloride and fluconazole assay levels.

    Product
    Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), 100 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India, NDC a)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1031-2018·2018-08-08

    Renaissance Lakewood Recalls Fluconazole Injection Bags Due to Stability Failures

    Renaissance Lakewood, LLC is recalling 3,000 bags of Fluconazole Injection due to elevated sodium chloride and water vapor levels.

    Product
    Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 400 mg in 200 mL (2 mg/mL), 200 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India; NDC 36000-003-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1032-2018·2018-08-08

    Fluconazole Injection Recalled for Elevated Water Vapor Levels

    Renaissance Lakewood, LLC is recalling Fluconazole Injection bags due to elevated water vapor levels. The recall covers 3,664 bags distributed nationwide and in Puerto Rico.

    Product
    Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), 100 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India, NDC 36000-002-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2598-2018·2018-08-08

    BD FACS Universal Loader Recalled for Insufficient Locking Mechanism

    Becton, Dickinson and Company is recalling 8 BD FACS Universal Loader devices because the solenoid plunger tip is too short to lock securely during use.

    Product
    BD FACS Universal Loader (Optional) to the BD FACSLyric Clinical System, Model 662879 (Universal Loader), Rx Only. The firm name on the label is Becton, Dickinson and Company, BD Biosciences, San Jose, CA. The Loader offers various settings to resuspend and mix samples. It…
    Category
    Medical Device
    Distribution
    6 states
  • SevereNHTSA·18V520000·2018-08-07

    Terex Recalls 2015-2018 Digger Derricks Due to Weld Defect

    Terex is recalling 2015-2018 C4000, C5000, C6000, and General 80 digger derricks because undersized welds may cause the auger to fall unexpectedly, posing an injury risk.

    Product
    TEREX — TEREX C6000, C4000, GENERAL 80, C5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V521000·2018-08-07

    BYD Recalls 2016-2017 K11 M Buses Due to Brake Caliper Defect

    BYD is recalling 2016-2017 K11 M hybrid buses because a brake caliper guide pin may break, potentially causing loss of braking ability or tire pressure.

    Product
    BYD — BYD K11 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V517000·2018-08-06

    Micro Bird Transit Bus Recall for Seat Belt Anchorage Defect

    Micro Bird is recalling 2015-2018 G5, MB II, and T-Series transit buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in crashes.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, T-SERIES TRANSIT BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V519000·2018-08-06

    Garden State Recalls 2015 Double Deck Buses for Emergency Exit Defect

    Garden State Bus Group is recalling 2015 Double Deck Buses because the roof emergency exit is incorrectly located, potentially delaying evacuation during an emergency.

    Product
    GARDEN STATE — GARDEN STATE DOUBLE DECK BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E079000·2018-08-06

    Hale Recalls Kubota Diesel Pumps Due to Wiring Defect

    Hale Products Inc is recalling Kubota Diesel Powered Portable Pumps because improper wiring may prevent warning lamps from illuminating, increasing the risk of injury if the engine fails.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V516000·2018-08-06

    Micro Bird Recalls 2015-2018 School Buses for Seat Belt Defect

    Micro Bird is recalling 2015-2018 G5, MB II, and T-Series school buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in a crash.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, MB II SCHOOL BUS, T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V518000·2018-08-06

    Newmar Recalls 2018-2019 Motorhomes Due to Door Latch Adjustment Issue

    Newmar is recalling 2018-2019 motorhomes because improperly adjusted door latch rods may allow the entry door to open during transit.

    Product
    NEWMAR — NEWMAR DUTCH STAR, VENTANA LE, VENTANA, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·066-2018·2018-08-03

    Star Natural Meats Recalls Raw Pork Sausage for Undeclared Allergens

    Star Natural Meats is recalling raw pork sausage products because they contain undeclared milk, soy, and restricted ingredients.

    Product
    Star Natural Meats LLC — Star Natural Meats, LLC Recalls Raw Pork Sausage Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V513000·2018-08-03

    Mercedes-Benz Recalls 2018 E 400 Cabrio for Child Seat Anchor Defect

    Mercedes-Benz is recalling 2018 E 400 Cabrio vehicles because the child seat anchoring system may not be properly installed, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V515000·2018-08-03

    Mercedes-Benz Recalls E-Class and CLS Models for Air Bag Calibration Issue

    Mercedes-Benz is recalling 2018 E-Class and 2019 CLS vehicles because the front passenger air bag may not deactivate if a child seat is installed, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 400, AMG E63S, E 300, E43 AMG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E078000·2018-08-03

    Honda Recalls Africa Twin Centerstand Kits Due to Detachment Risk

    Honda is recalling Genuine Accessory Centerstand Kits for 2016-2018 Africa Twin motorcycles because a broken circlip can cause the stand to detach, creating a road hazard or causing the bike to fall.

    Product
    HONDA — HONDA CRF1000A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V512000·2018-08-03

    Mercedes-Benz Recalls 2018 GLE Models for Sunroof Adhesion Defect

    Mercedes-Benz is recalling 2018 GLE 350 and AMG GLE43 vehicles because the panoramic sunroof may not be properly adhered, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, AMG GLE43
    Category
    Vehicle
    Distribution
    Distributed nationwide