The Recall Desk

State

Kansas product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37201–37225 of 79562

  • ModerateFDA (Devices)·Z-1035-2019·2019-03-27

    ConvaTec Recalls Forceps Blue Due to Potential Sterile Barrier Breach

    ConvaTec, Inc. is recalling Forceps Blue, disposable sterile forceps, because an internal assessment confirmed the potential for a breach in the sterile barrier.

    Product
    Forceps Blue, disposable, sterile, 100 eaches per sales unit. Product Usage: Forceps are sterile disposable devices intended for use during clinical procedures to grasp, manipulate, maneuver or assist with the removal of debris, particulates or wound tissue. Typically…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1032-2019·2019-03-27

    ACell Recalls Gentrix Surgical Matrix Thick Due to Tensile Strength Failure

    ACell, Inc. is recalling one lot of Gentrix Surgical Matrix Thick devices because a sample failed to meet tensile strength specifications.

    Product
    Gentrix Surgical Matrix Thick, 30 x 40cm, Catalog Number PSMT3040, Lot 013948 - Product Usage: Gentrix Surgical Matrix Thick is intended for implantation to reinforce soft tissue where weakness exists in patients requiring gastroenterological or plastic and reconstructive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1024-2019·2019-03-27

    Cook Medical Recalls Celect Platinum Vena Cava Filters for Labeling Updates

    Cook Medical is recalling Celect Platinum Vena Cava Filter Sets to update the Instructions for Use. The recall affects 9,173 units distributed nationwide.

    Product
    Cook Celect Platinum Vena Cava Filter Set for Femoral Vein Approach, Catalog Number IGTCFS-65-1-FEM-CELECT-PT Product Usage: The Cook Celect Platinum Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1034-2019·2019-03-27

    Agfa Radiographic Film Recalled for Visible Pinholes in Images

    Agfa N.V. is recalling specific lots of PET Plates Coated Film-MONOMEDBV2S2 radiographic film because inhomogeneous coating solutions cause visible pinholes in images.

    Product
    PET Plates Coated Film-MONOMEDBV2S2- Radiographic Film REF: XJUB8, XJM73, XJUDD, XJM85, EKLYZ. Product Usage: Due to an inhomogeneous coating solution, pinholes can become visible in even dark images. Visibility of the pinholes varies as material from this coating run…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1026-2019·2019-03-27

    Cook Medical Recalls Celect Platinum Vena Cava Filters for Labeling Updates

    Cook Medical is recalling Celect Platinum Vena Cava Filter Sets to update the Instructions for Use. The recall affects 9,173 units distributed nationwide.

    Product
    Cook Celect Platinum Vena Cava Filter Set for Femoral and Jugular Vein Approach, Catalog Number IGTCFS-65-1-UNl-C ELECT-PT Product Usage: The Cook Celect Platinum Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1023-2019·2019-03-27

    Cook Medical Recalls Gunther Tulip Vena Cava Filters for Labeling Updates

    Cook Medical is recalling 9,173 Gunther Tulip Vena Cava Filter Sets to update the Instructions for Use. The products were distributed nationwide.

    Product
    Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach, Catalog Number IGTCFS-65-1-UNl-TULIP Product Usage: The Gunther Tulip Filter is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1025-2019·2019-03-27

    Cook Medical Recalls Celect Platinum Vena Cava Filters for Labeling Updates

    Cook Medical is recalling Celect Platinum Vena Cava Filters to update the Instructions for Use. The recall affects 9,173 units distributed nationwide.

    Product
    Cook Celect Platinum Vena Cava Filter Set for Jugular Vein Approach, Catalog Number GTCFS-65-1-JUG-CELECT-PT Product Usage: The Cook Celect Platinum Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1022-2019·2019-03-27

    Cook Medical Recalls Gunther Tulip Vena Cava Filters for Labeling Updates

    Cook Medical is recalling 9,173 Gunther Tulip Vena Cava Filter Sets to update the Instructions for Use. The products were distributed nationwide.

    Product
    Gunther Tulip Vena Cava Filter Set for Jugular Vein Approach, Catalog Number IGTCFS-65-1-JUG-TULIP Product Usage: The Gunther Tulip Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following situations…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1021-2019·2019-03-27

    Cook Medical Recalls Gunther Tulip Vena Cava Filters for Labeling Updates

    Cook Medical is recalling 9,173 Gunther Tulip Vena Cava Filter Sets to update the Instructions for Use.

    Product
    Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach, Catalog Number IGTCFS-65-1-FEM-TU LIP Product Usage: The Gunther Tulip Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·19090·2019-03-26

    Universal Rechargeable Power Banks Recalled Due to Fire Hazard

    Daniel M. Friedman & Associates is recalling about 170,500 universal rechargeable power banks due to a fire hazard. The devices can overheat, causing property damage.

    Product
    Universal rechargeable power banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V238000·2019-03-26

    Vantage Recalls Shuttle Vehicles with Defective Foldaway Seat Locks

    Vantage Mobility is recalling specific shuttle vehicles equipped with Freedman GO-3S foldaway seats because the seat cushion may not remain locked in place during a crash or sudden stop.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FORD, FREIGHTLINER SPRINTER 3500, SPRINTER 2500, TRANSIT, F-250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V239000·2019-03-26

    Custom Fab & Body Recalls Emergency Vehicles with Faulty Brake Lights

    Custom Fab & Body is recalling specific 2017-2018 emergency vehicles because Whelen brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    KENWORTH — KENWORTH, FORD, INTERNATIONAL T370, F-650 SD, WORKSTAR, DURASTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V233000·2019-03-25

    North American Repower Recalls One 2005 International 1652SC CNG Vehicle

    North American Repower is recalling one 2005 International 1652SC vehicle due to a potential CNG valve defect that could cause stem ejection, injury, or fire.

    Product
    INTERNATIONAL — INTERNATIONAL 1652SC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V234000·2019-03-25

    Daimler Recalls 2019-2020 Thomas Built C2 School Buses for Steering Hose Issue

    Daimler Trucks North America is recalling 2019-2020 Thomas Built C2 Saf-T-Liner school buses because a steering hose clamp may be improperly installed, risking loss of steering assist.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V232000·2019-03-25

    BFX Fire Apparatus Recalls 2017-2018 Brush Trucks for Brake Light Defect

    BFX Fire Apparatus is recalling 55 units of 2017-2018 Brush Trucks because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    BFX FIRE APPARATUS — BFX FIRE APPARATUS BRUSH TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V230000·2019-03-25

    KME Commercial Rescue and Tanker Vehicles Recalled for Camera Display Defect

    KME is recalling 2017 Commercial Rescue and 2019 Commercial Tanker vehicles because the backup camera display may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    KME — KME COMMERCIAL RESCUE, COMMERCIAL TANKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·037-2019·2019-03-23

    North Country Smokehouse Recalls Kielbasa Sausage Due to Metal Contamination

    North Country Smokehouse is recalling ready-to-eat kielbasa sausage products that may contain metal. The recall affects approximately 2,686 pounds shipped to retail locations nationwide.

    Product
    North Country Smokehouse — North Country Smokehouse Recalls Ready-To-Eat Sausage Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V224000·2019-03-22

    Fleetwood and Holiday Rambler Motorhomes Recalled for Battery Fire Risk

    REV Recreation Group is recalling 2019 Fleetwood Flair and Holiday Rambler Admiral motorhomes because battery straps may cause a short circuit and fire.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FLAIR, ADMIRAL
    Category
    Vehicle
    Distribution
    Distributed nationwide