The Recall Desk

State

Kansas product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54426–54450 of 79655

  • ModerateFDA (Devices)·Z-0738-2016·2016-02-10

    Horiba ABX PENTRA Cholesterol CP Reagent Recalled for Interference

    Horiba Instruments Inc is recalling 216 units of ABX PENTRA Cholesterol CP reagent because N-acetylcysteine can cause falsely low results.

    Product
    The ABX PENTRA Cholesterol CP ref. A11A01634 is an in vitro diagnostic assay for quantitative determination of cholesterol in human serum and plasma based on an enzymatic photometric test (Trinders reaction). The assay is composed of a 99 ml mono-reagent cassette. Reagent is a…
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-0754-2016·2016-02-10

    Siemens ADVIA Centaur PSA Assay Recalled for High Dose Hook Effect Failure

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur PSA Assay kits because they do not meet the High Dose Hook Effect expectation in the Instructions for Use.

    Product
    ADVIA Centaur PSA Assay; Catalog Number: 06574155/SMN 10310292 (100 test kit) and Catalog Number: 02676506/SMN 10310293 (500 test kit) Product Usage: This in vitro diagnostic assay is intended to quantitatively measure prostate-specific Antigen (PSA) in human serum using the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0651-2016·2016-02-10

    Perrigo Recalls Nystatin Powder for Labeling Error on Declared Strength

    Perrigo Company PLC is recalling Nystatin, USP Powder for Rx compounding due to a labeling error regarding the declared strength.

    Product
    Nystatin, USP Powder for Rx compounding, 50 Million Units, Packaged by Perrigo, Minneapolis MN 55427, NDC 0574-0405-05, UPC 305740404058.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0742-2016·2016-02-10

    Horiba Instruments Recalls ABX PENTRA Triglycerides Assay Due to Interference

    Horiba Instruments Inc is recalling ABX PENTRA Triglycerides CP assays because N-acetylcysteine in patient blood can cause falsely low results.

    Product
    ABX PENTRA Triglycerides CP ref. A11A01640 is an in vitro diagnostic assay for the quantitative determination of triglycerides in human serum and plasma based on an enzymatic colorimetric test. It is composed of a 99 ml mono-reagent cassette. Reagent is a chemical solution with…
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-0740-2016·2016-02-10

    Horiba ABX PENTRA Glucose Reagent Recalled for NAC Interference

    Horiba Instruments Inc is recalling ABX PENTRA Glucose reagents because N-acetylcysteine in patient blood can cause falsely low glucose results.

    Product
    ABX PENTRA Glucose PAP CP ref. A11A01668 reagent is intended for the quantitative in vitro diagnostic determination of glucose in human serum, plasma and urine using glucose oxidase method by colorimetry.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-0731-2016·2016-02-10

    Baxter RAPIDFILL Syringe Strips Recalled for Shelf Life Packaging Claim

    Baxter is recalling RAPIDFILL Syringe Strips because the packaging claims a 12-month shelf life without supporting evidence.

    Product
    Baxter, RAPIDFILL Syringe Strip, 10 ml. For use with RAPIDFILL Automated Syringe Filler (ASF)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0650-2016·2016-02-10

    Mylan Recalls Clonazepam Tablets Due to Impurity Specification Failure

    Mylan Institutional, Inc. is recalling Clonazepam Tablets, 0.5 mg, because a known impurity exceeded specifications at the 6-month timepoint.

    Product
    Clonazepam Tablets, USP, 0.5 mg, 100-count carton, Rx only, Manufactured by Mylan Pharmaceuticals Inc., Morgantown, WV, 26505, NDC:51079-881-21
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V074000·2016-02-09

    Honda Recalls 2016 Civics Due to Engine Piston Defect

    Honda is recalling 2016 Civic vehicles with 2.0L engines because missing or incorrect piston circlips may cause engine seizure, increasing the risk of a crash or fire.

    Product
    HONDA — HONDA CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E011000·2016-02-09

    Haier Recalls 55-Inch LED Televisions in Fifth-Wheel Recreational Vehicles

    Haier is recalling 55-inch LED televisions installed in fifth-wheel recreational vehicles because mounting brackets may separate, causing the TVs to fall.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V066000·2016-02-05

    Peterbilt Recalls 2015-2016 Trucks Due to Drive Axle Nut Defect

    PACCAR is recalling 2015-2016 Peterbilt 365 and 367 trucks because improperly tightened drive axle nuts may cause the driveshaft to disconnect, increasing crash risk.

    Product
    PETERBILT — PETERBILT 367, 365
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V071000·2016-02-05

    BMW Recalls Vehicles Due to Driver Air Bag Inflator Rupture Risk

    BMW is recalling approximately 840,000 vehicles because the driver's frontal air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    BMW — BMW 128I, X6 SAC, X5 SAV, 135I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V069000·2016-02-05

    GM Recalls 2015-2016 Trucks and SUVs for Brake Pedal Defect

    General Motors is recalling specific 2015-2016 Chevrolet and GMC trucks and SUVs because the brake pedal pivot nut may loosen, potentially making the brake pedal inoperative.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 2500, SIERRA 3500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V065000·2016-02-05

    Toyota and Lexus Vehicles Recalled for Side Air Bag Defect

    Toyota is recalling specific 2003-2006 Land Cruiser, LX470, Tundra, Sequoia, 4Runner, and GX470 vehicles because side air bags may deploy unexpectedly, increasing injury risk.

    Product
    LEXUS — LEXUS, TOYOTA LX470, GX470, 4RUNNER, LAND CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V070000·2016-02-05

    Kia Recalls 2011 Fortes for Transmission Fluid Leak Risk

    Kia is recalling 2011 Fortes because a defective transmission cooler hose may leak fluid, potentially causing the vehicle to stop moving and increasing crash risk.

    Product
    KIA — KIA FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16096·2016-02-04

    CE North America Recalls KUL Fan Heaters Due to Fire Hazard

    CE North America is recalling KUL portable fan heaters sold at Bed Bath & Beyond because they can overheat and catch fire. Four fire incidents have been reported, with no injuries.

    Product
    KUL Fan Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E009000·2016-02-04

    Takata Recalls Side Air Bag Inflators Due to Rupture Risk

    Takata is recalling specific side air bag inflators manufactured in December 2014 because a manufacturing error could cause them to rupture and propel metal fragments into the vehicle.

    Product
    AIR BAGS:SIDE/WINDOW recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16095·2016-02-04

    Wedgwood Decorative Baby Rattles Recalled Due to Choking Hazard

    WWRD is recalling Wedgwood Peter Rabbit decorative baby rattles because ball bearings can release, posing a choking hazard to young children.

    Product
    Wedgwood Peter Rabbit decorative baby rattles
    Category
    Consumer Product
    Distribution
    Distributed nationwide