The Recall Desk

State

Kansas product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48501–48525 of 79646

  • ModerateFDA (Devices)·Z-1048-2017·2017-01-25

    Endologix AFX Endovascular AAA System Recall for Updated Endoleak Information

    Endologix is recalling 34 units of the AFX Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.

    Product
    AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75 V F0070308 A2828/C75 V F0070312 A3434/C80 V f00553 I1616/C55F SA F00556 I2013/C70F SA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1045-2017·2017-01-25

    DICOM GRID Recalls Ambra PACS Software Due to Image Display Error

    DICOM GRID Inc. is recalling Ambra PACS software version V3.16.13.0 because a defect causes diagnostic images to appear washed out, potentially affecting image analysis.

    Product
    Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 Intended for use as a primary diagnostic and analysis tool for diagnostic images.
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-1041-2017·2017-01-25

    Smith & Nephew RENASYS GO Wound Therapy Recall for Clearance Issue

    Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy devices because they lack 510(k) clearance for a design modification.

    Product
    Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy, Rx only. Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious materials. Used for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1042-2017·2017-01-25

    Smith & Nephew RENASYS GO Power Supply Recalled for Regulatory Clearance

    Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy External Power Supply Units because they lack 510(k) clearance for a design modification.

    Product
    Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy External Power Supply Unit, Rx only. Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0433-2017·2017-01-25

    Novum Pharma Recalls Subpotent Novacort Gel Sample Packets

    Novum Pharma is recalling Novacort Gel sample packets because the pramoxine hydrochloride content was found to be out of specification.

    Product
    Novacort Gel Sample Packets (2% hydrocortisone acetate, 1% pramoxine HCl), 10-count Carton of 1.0 g sample packets), NDC 69646-704-38 (10 ct. Carton of 1gm samples) / NDC 69646-704-01 (Individual 1gm Samples within Carton), Rx Only, Novum Pharma LLC, Chicago, IL 60654
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1030-2017·2017-01-25

    Exactech Recalls Novation Cemented Plus Femoral Stems Due to Labeling Error

    Exactech is recalling 79 Novation Cemented Plus Femoral Stems because they were labeled with incorrect Global Trade Item Numbers (GTINs).

    Product
    Novation Cemented Plus Femoral Stem, 12/14, Collared, Standard Offset, Matte, Cemented, Size 15.
    Category
    Medical Device
    Distribution
    13 states
  • LowFDA (Drugs)·D-0431-2017·2017-01-25

    Teva Recalls Risedronate Sodium Tablets for Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling 6,800 cartons of Risedronate Sodium Delayed-release Tablets, 35 mg, because they failed dissolution specifications.

    Product
    Risedronate Sodium Delayed-release Tablets, 35 mg, Once-a-Week, 1 tablet per blister (NDC 0093-5509-19), packaged in 4 blisters per carton (NDC 0093-5509-44), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V052000·2017-01-24

    Ford Recalls 2016 Focus and C-Max for Floor Pan Welding Defect

    Ford is recalling 2016 Focus and C-Max vehicles because improperly welded floor pan joints may reduce structural integrity, increasing injury risk in a crash.

    Product
    FORD — FORD FOCUS, C-MAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17071·2017-01-24

    HP Recalls Lithium-Ion Notebook Batteries Due to Fire and Burn Hazards

    HP is expanding a recall of about 101,000 lithium-ion batteries for HP and Compaq notebook computers because they can overheat, posing fire and burn risks.

    Product
    Lithium-ion batteries used in HP notebook computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V051000·2017-01-24

    Toyota Recalls 2016-2017 Tundra Trucks for Rear Bumper Defect

    Toyota is recalling 2016-2017 Tundra trucks with resin rear bumpers because the brackets may break if stepped on, posing an injury risk.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V053000·2017-01-24

    Ford Recalls 2017 F-150 Trucks Due to Instrument Cluster Power Loss

    Ford is recalling 2017 F-150 trucks because the instrument cluster may lose power in cold weather, potentially hiding the transmission gear position and increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V050000·2017-01-23

    Autocar Recalls 2013-2016 Xpeditor Trucks Due to Brake Defect

    Autocar is recalling 38 Xpeditor trucks from 2013-2016 because over-braking can cause S-cam tube bolts to loosen, leading to unexpected brake engagement and increased crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E005000·2017-01-23

    IH Parts Recalls Steering Tie Rod Adjusters for Fracture Risk

    IH Parts America Inc. is recalling specific steering tie rod adjusters for International Scout vehicles because they may fracture, affecting steering capability and increasing crash risk.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17V047000·2017-01-20

    BMW Recalls 2000-2003 Models for Driver Air Bag Inflator Rupture Risk

    BMW is recalling specific 2000-2003 3, 5, and X5 series vehicles because replacement driver-side air bag inflators may rupture during deployment, posing a risk of serious injury or death.

    Product
    BMW — BMW 323, 320, 325, 330
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V048000·2017-01-20

    Walker Recalls 2014-2017 Food Grade Tank Trailers for Underride Guard Defect

    Walker is recalling 2014-2017 Food Grade Tank Trailers because weld joints on the underride guard may crack, potentially causing the guard to detach and become a road hazard.

    Product
    WALKER — WALKER FOOD GRADE TANK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V046000·2017-01-20

    Maserati Recalls 2014-2017 Models for Seat Wiring Fire Risk

    Maserati is recalling 39,381 vehicles due to a front seat wiring harness defect that may cause an electrical short and increase the risk of a fire.

    Product
    MASERATI — MASERATI QUATTROPORTE, GHIBLI, LEVANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2017·2017-01-20

    Hans Kissle Recalls Ready-To-Eat Chicken Bowls Due to Processing Defect

    Hans Kissle Company is recalling approximately 6,348 pounds of ready-to-eat chicken bowls due to a potential process defect that could allow bacterial pathogens to survive.

    Product
    Hans Kissle Company, LLC — Hans Kissle Company, LLC. Recalls Ready-To-Eat Chicken Products Due To Potential Processing Deviation
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17E004000·2017-01-20

    New Haven Recalls Wheelchair Securement Tiedowns Due to Crash Risk

    The New Haven Companies is recalling Safe Haven Wheelchair Securement Tiedowns because they may not adequately secure a wheelchair in a crash, increasing injury risk.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V044000·2017-01-20

    Airstream Recalls 2017 Trailers Due to Incorrect Tire Certification Labels

    Airstream is recalling 2017 Sport, International, and Flying Cloud trailers because incorrect tire labels could lead to overinflation and tire blowouts.

    Product
    AIRSTREAM — AIRSTREAM SPORT, INTERNATIONAL, FLYING CLOUD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·008-2017·2017-01-19

    Mountain View Packaging Recalls Sweet Chili Chicken Due to Undeclared Allergens

    Mountain View Packaging is recalling 1,080 pounds of sweet chili chicken products because they contain undeclared wheat, egg, and milk allergens.

    Product
    Mountain View Packaging, LLC — Mountain View Packaging, LLC Recalls Chicken Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V041000·2017-01-19

    Pratt Recalls 2014 ISO Tank Chassis Due to Axle Spindle Defect

    Pratt Industries is recalling 126 units of 2014 DC432LS9 and DC432LS9HL ISO Tank Chassis because a defective axle spindle may cause the wheel end to separate, increasing crash risk.

    Product
    PRATT — PRATT DC432LS9 ISO TANK CHASSIS, DC432LS9HL ISO TANK CHASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17070·2017-01-19

    Trek Recalls 720 Disc Bicycles Due to Wheel Spoke Fall Hazard

    Trek is recalling 720 Disc bicycles and wheel sets because broken spokes can contact the brake caliper, posing a fall hazard to riders.

    Product
    Trek 720 Disc bicycles and wheel sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide