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.

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.

49826–49850 of 79646

  • HighNHTSA·16E081000·2016-10-28

    Vega Motorcycle Helmets Recalled for Failing Federal Safety Standards

    Vega Helmet Corporation is recalling specific XTA and XTA Touring half helmets because they may not adequately protect the wearer's head in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V787000·2016-10-28

    Forest River Recalls 2017 Salem and Wildwood Trailers for Labeling Errors

    Forest River is recalling 92 model year 2017 Salem and Wildwood recreational trailers because the Federal Placard Label and VIN incorrectly state the vehicles have two axles instead of one.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V786000·2016-10-28

    Starcraft RV Recalls 2017 AR-ONE Trailers for Incorrect Load Labels

    Starcraft RV is recalling 94 model year 2017 AR-ONE trailers because incorrect Federal Placard and Cargo Carrying Capacity labels may lead to overloading and increased crash risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V784000·2016-10-27

    Holiday Rambler Vacationer Motorhomes Recalled for Front Truss Support Defect

    REV Recreation Group is recalling 2015-2016 Holiday Rambler Vacationer motorhomes because a front truss may not be adequately supported, risking wire or hydraulic line damage.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER VACATIONER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V785000·2016-10-27

    Jayco Recalls 2017 Jay Sport Trailers Due to Incorrect Tire Labels

    Jayco is recalling 2017 Jay Sport camping trailers because tire labels list the wrong tire size and pressure, which could lead to over-inflation and tire failure.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY SERIES SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0147-2017·2016-10-26

    Good Earth Egg Company Recalls Shell Eggs Due to Salmonella Risk

    Good Earth Egg Company is recalling shell eggs that may be contaminated with Salmonella. The product was distributed to customers in Georgia, Illinois, Kansas, and Missouri.

    Product
    Shell eggs, various sizes, packaged in the following ways: 6-count cartons, 10-count cartons, 12-count cartons, 18-count cartons, 15 dozen cases, and 30 dozen cases; under the brand name Good Earth Egg Company and MO license # D-01124. The responsible firm name is Good Earth…
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·16V779000·2016-10-26

    Ford Recalls 2015-2017 Mustangs for Engine Oil Cooler Hose Defect

    Ford is recalling 2015-2017 Mustangs because an engine oil cooler hose may separate, causing an oil leak that could lead to engine failure or fire.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0177-2017·2016-10-26

    Dollar General Recalls Mold-Contaminated Soft Baked Chocolate Brownie Cookies

    Dollar General is recalling Soft Baked Chocolate Brownie Cookies due to the presence of mold. Consumers should discard the product or return it for a refund.

    Product
    Cookies Bergen, Soft Baked Chocolate Brownie Cookies, NET WEIGHT: 4.44 OZ (126g), Produced by P.W. Sponmet Sp.l., Poland
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0231-2017·2016-10-26

    Windstone Medical Recalls Major General Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 852 Major General Packs because Medtronic gloves inside may have splits or holes that compromise sterility.

    Product
    Major General Pack, Kit number 002645-11 and 002645-12 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0260-2017·2016-10-26

    Windstone Medical Packaging Recalls Peri Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 115 Peri Kits (PSS1037) because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Peri Kit, Kit number PSS1037 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0054-2017·2016-10-26

    Vascular Solutions Recalls Twin-Pass RX Dual Access Catheters Due to Manufacturing Defect

    Vascular Solutions is recalling Twin-Pass RX Dual Access Catheters because excess manufacturing material may remain at the tip or within the distal lumen.

    Product
    Vascular Solutions Twin-Pass RX Dual Access Catheter, model 5210. Sterilized with Ethylene Oxide. The Twin-Pass dual access catheter is a dual lumen catheter designed for use in the coronary and/or peripheral vasculature. The Twin-Pass catheter (Models 5200 and 5230)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0141-2017·2016-10-26

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility in custom surgical kits.

    Product
    Anterior Cervical Fusion Pack, Kit part numbers: AMS2502 and AMS2502(A convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0274-2017·2016-10-26

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because they may contain splits or holes that compromise sterility.

    Product
    Taymour GYN Pack, Kit number PSS2642 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0053-2017·2016-10-26

    Vascular Solutions Recalls Twin-Pass Catheters Due to Manufacturing Material

    Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the tip or in the distal lumen.

    Product
    Vascular Solutions Twin-Pass Dual Access Catheter, models 5200, 5210, and 5230. Sterilized with Ethylene Oxide. The Twin-Pass dual access catheter is a dual lumen catheter designed for use in the coronary and/or peripheral vasculature. The Twin-Pass catheter (Models 5200…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V777000·2016-10-26

    Ford Recalls 2010-2012 Escape and 2010-2011 Mariner for Fuel Leak Risk

    Ford is recalling specific 2010-2012 Escape and 2010-2011 Mariner vehicles because a cracked fuel delivery module may cause a fuel leak, increasing the risk of fire.

    Product
    FORD — FORD, MERCURY ESCAPE, MARINER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0212-2017·2016-10-26

    Del Monte Recalls Cut Green Beans Due to Crawfish Parts

    Del Monte is recalling cut green beans and field peas with snaps due to a customer complaint of finding crawfish parts in the product.

    Product
    Cut Green Beans packed under brand names of: Allens Cut Green Beans (Ejotes Cortados Lago Azul) Blue Lake . Allens Cracker Barrel Label (Both labels have same UPC # - different sodium content - 140 mg for Allens Cut Green Beans and 250 for Cracker Barrel label Peso Neto…
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-0005-2017·2016-10-26

    Heartware Ventricular Assist System Controller Recall for Loose Connector Ports

    Heartware, Inc. is recalling Ventricular Assist System Controllers due to loose connector ports. The recall affects 4,235 units worldwide, including 7,272 in the U.S.

    Product
    HeartWare Ventricular Assist System Controller Product Usage: For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HVAD is designed for in-hospital and out-of-hospital settings…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0213-2017·2016-10-26

    Del Monte Recalls Field Peas and Green Beans Due to Crawfish Parts

    Del Monte is recalling approximately 15,000 cases of canned field peas and green beans after a customer complaint reported finding crawfish parts in the product.

    Product
    Allens East Texas Fair Brand, Tiny Tender Field Peas with snaps; NET.WT. 6 lbs. 15 oz.. (3.15kg) UPC 0 34700 623214 8 Distributed by Sager Creek Vegetable Company, Siloam Springs, AR 72761-0250 USA; UPC 0 34700 63213 1
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-0055-2017·2016-10-26

    Vascular Solutions Recalls Twin-Pass Dual Access Catheters Due to Manufacturing Residue

    Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the catheter tip or within the distal rapid exchange lumen.

    Product
    Vascular Solutions Twin-Pass .023" Dual Access Catheter, model 5230. Sterilized with Ethylene Oxide. The Twin-Pass dual access catheter is a dual lumen catheter designed for use in the coronary and/or peripheral vasculature. The Twin-Pass catheter (Models 5200 and 5230)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V778000·2016-10-26

    Ford Recalls 2017 F-Series Trucks Due to Fuel Leak Fire Risk

    Ford is recalling 2017 F-250 through F-550 Super Duty trucks because a fuel shield may detach, causing a leak that increases fire risk.

    Product
    FORD — FORD F-550 SD, F-350 SD, F-450 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide