The Recall Desk

State

Kansas product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51026–51050 of 79649

  • HighNHTSA·16V623000·2016-08-26

    Tiffin Allegro Recall: Driver-Side Wiper Arm May Break

    Tiffin is recalling 2017 Allegro Open Roads because the driver-side wiper arm may break, reducing visibility and increasing crash risk.

    Product
    TIFFIN — TIFFIN ALLEGRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V621000·2016-08-25

    Ford Recalls 2013-2015 Taurus, Flex, MKS, MKT for Fuel Pump Defect

    Ford is recalling 2013-2015 Taurus, Flex, MKS, and MKT vehicles because a fuel pump component may overheat, causing the engine to stall or preventing the vehicle from starting.

    Product
    LINCOLN — LINCOLN, FORD MKS, FLEX, MKT, TAURUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16253·2016-08-25

    Whirlpool Recalls Microwave Hood Combinations Due to Fire Hazard

    Whirlpool is recalling about 15,200 microwave hood combinations because internal arcing can ignite plastic components, posing a fire hazard.

    Product
    Whirlpool brand microwave hood combinations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16251·2016-08-25

    M&M's Branded Jewelry Recalled for Lead Content Violations

    Mars Retail Group is recalling M&M's-branded jewelry due to high lead levels. Consumers should stop using the items and return them for a refund.

    Product
    M&M'S®-branded jewelry
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V622000·2016-08-25

    Bison Recalls 2015-2016 Horse Trailers Due to Missing Battery Fuse

    Bison Coach is recalling 654 model year 2015-2016 horse trailers because a missing inline fuse on the battery cable could cause overheating and fire during an electrical short.

    Product
    BISON — BISON RANGER, SILVERADO, TRAIL BOSS, TRAIL HAND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16252·2016-08-25

    Cree Recalls LED T8 Lamps Due to Overheating and Burn Hazard

    Cree is recalling LED T8 replacement lamps that can overheat and melt, posing a burn hazard. No injuries have been reported.

    Product
    Cree® LED T8 Replacement Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V620000·2016-08-25

    Seagrave Recalls Marauder II Fire Trucks Due to Transmission Defect

    Seagrave is recalling 28 Marauder II fire trucks because a transmission component may fail, preventing the vehicle from pumping water at fire scenes.

    Product
    SEAGRAVE — SEAGRAVE MARAUDER II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2533-2016·2016-08-24

    Baxter Recalls VASCU-GUARD Patches Due to Bleeding Reports

    Baxter Healthcare is recalling VASCU-GUARD Peripheral Vascular Patches due to postmarketing reports of intraoperative and postoperative bleeding, including one fatal outcome.

    Product
    Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and product codes: 1 cm x 6 cm, product code VG0106N, 0.8 cm x 8 cm, product code VG0108N, 1 cm x 10 cm, product code VG0110N, and 2 cm x 9 cm, product code VG0209N. VASC U-GUARD is prepared from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1933-2016·2016-08-24

    HelloFresh Recalls Lemony Pan-Seared Chicken Meal Due to Listeria Risk

    HelloFresh is recalling Lemony Pan-Seared Chicken with Pesto Potato Salad and Peas due to possible Listeria monocytogenes contamination.

    Product
    Lemony Pan-Seared Chicken with Pesto Potato Salad and Peas
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1935-2016·2016-08-24

    HelloFresh Recalls Lamb-Stuffed Zucchini Due to Listeria Risk

    HelloFresh is recalling 1,258 pounds of Nir's Lamb-Stuffed Zucchini with Spiced Lentil Stew due to possible Listeria monocytogenes contamination.

    Product
    Nir's Lamb-Stuffed Zucchini with Spiced Lentil Stew
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1934-2016·2016-08-24

    HelloFresh Recalls Seared Steak Meal Due to Listeria Risk

    HelloFresh is recalling Seared Steak with Spring Veggie Succotash and Mint-Chive Pesto due to possible Listeria monocytogenes contamination.

    Product
    Seared Steak with Spring Veggie Succotash and Mint-Chive Pesto
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Drugs)·D-1458-2016·2016-08-24

    Golden State Medical Supply Recalls Venlafaxine Hydrochloride Extended-Release Capsules

    Golden State Medical Supply Inc. is recalling specific lots of Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, due to failed dissolution specifications.

    Product
    Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, a) 30 capsules per bottle, NDC # 60429-123-30, b) 90 capsules per bottle, NDC # 60429-123-90, Rx Only, GSMS.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2567-2016·2016-08-24

    Medtronic Valleylab Laparoscopic Electrode Recalled for Sterile Barrier Compromise

    Medtronic is recalling Valleylab Laparoscopic Flat L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 119,770 units distributed worldwide.

    Product
    Valleylab Laparoscopic Flat L-Hook Electrode 36CM Item Code: E277436 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction via a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1922-2016·2016-08-24

    Newly Weds Foods Recalls Flour Breader Contaminated with E. coli O121

    Newly Weds Foods Inc is recalling bulk flour bland breader contaminated with E. coli O121. The product was distributed nationwide in 15, 30, and 50 lb bags or boxes.

    Product
    Bulk flour bland breader packaged into 15, 30, and 50 lb bags or boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2575-2016·2016-08-24

    Medtronic Valleylab Laparoscopic Electrode Recall for Sterile Barrier Compromise

    Medtronic is recalling Valleylab Laparoscopic Wire L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 50,055 units distributed worldwide.

    Product
    Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code: E2783R36ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1932-2016·2016-08-24

    HelloFresh Recalls Summer Vegetable Salad Due to Listeria Risk

    HelloFresh is recalling Summer Vegetable Salad with Seared Chicken due to possible Listeria monocytogenes contamination. The product was distributed in 28 states.

    Product
    Summer Vegetable Salad with Seared Chicken, Garlic Croutons, and Mustard-Chive Vinaigrette
    Category
    Food
    Distribution
    28 states
  • HighFDA (Devices)·Z-2577-2016·2016-08-24

    Medtronic Recalls Laparoscopic Electrode Due to Sterile Barrier Compromise Risk

    Medtronic is recalling 3,470 Valleylab Laparoscopic Flat L-Hook Electrodes because the package may be compromised, potentially breaching the sterile barrier.

    Product
    Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code: E2784R28ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2572-2016·2016-08-24

    Medtronic Recalls Laparoscopic Electrodes Due to Sterile Barrier Compromise

    Medtronic is recalling 1,440 Valleylab Laparoscopic Wire J-Hook Electrodes because the packaging may be compromised, potentially breaching the sterile barrier.

    Product
    Valleylab Laparoscopic Wire J-Hook Electrode Retractable 28CM Item Code: E2782R28ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2582-2016·2016-08-24

    Synthes Recalls Titanium Single Vector Distractor Bodies Due to Fastener Separation Risk

    Synthes (USA) Products LLC is voluntarily recalling 182 units of Titanium Single Vector Distractor Bodies because the fastener may separate prematurely from the Proximal Foot Plate.

    Product
    TI Single Vector Distractor Body with Left Foot/20mm; Catalog ID 487.963 The Titanium Single Vector Distractor and Proximal Foot Plates are intended for mandibular bone lengthening where gradual bone distraction is required, including conditions such as congenital mandibular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2581-2016·2016-08-24

    Synthes Recalls Titanium Single Vector Distractor Bodies Due to Fastener Separation Risk

    Synthes (USA) Products LLC is voluntarily recalling 90 units of Titanium Single Vector Distractor Bodies because the fastener may separate prematurely from the Proximal Foot Plate.

    Product
    TI Single Vector Distractor Body with Right Foot/20mm; Catalog ID 487.962 The Titanium Single Vector Distractor and Proximal Foot Plates are intended for mandibular bone lengthening where gradual bone distraction is required, including conditions such as congenital mandibular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V615000·2016-08-24

    Hyundai Recalls 2016 Sonata Vehicles Due to Driver Air Bag Defect

    Hyundai is recalling specific 2016 Sonata vehicles because the driver-side frontal air bag may not adequately protect the driver's neck in a crash.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2555-2016·2016-08-24

    Medtronic Recalls Valleylab Laparoscopic Argon Electrodes Due to Sterile Barrier Risk

    Medtronic is recalling 19,200 Valleylab Laparoscopic Flexible Argon Electrodes because the packaging may be compromised, potentially breaching the sterile barrier.

    Product
    Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 3" Item Code: E25303 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1916-2016·2016-08-24

    Kerry Inc. Recalls Jalapeño Breader Due to E. coli O121 Contamination Risk

    Kerry Inc. is recalling Golden Dipt Jalapeño Breader because it was made with flour potentially contaminated with E. coli O121.

    Product
    Golden Dipt¿ Jalape¿o Breader is in a white 10 pound bag with the UPC number 763089721548 and Item Number: G5620.690.
    Category
    Food
    Distribution
    9 states