The Recall Desk

State

Kansas product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30526–30550 of 79543

  • ModerateFDA (Devices)·Z-2639-2020·2020-07-22

    Neocis Gen 2 Anterior Chairside Splint Recalled for Mislabeled Packaging

    Neocis Inc. is recalling 50 units of Gen 2 Anterior Chairside Splints due to potential mislabeling. The affected products are distributed nationwide.

    Product
    DRW-0742-01: Gen 2 Anterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1391-2020·2020-07-22

    Fresenius Kabi Recalls Fosaprepitant Injection Due to Labeling Error

    Fresenius Kabi USA, LLC is recalling 63,067 vials of Fosaprepitant for Injection because carton labels and product inserts incorrectly state the amount of the excipient edetate disodium (EDTA).

    Product
    FOSAPREPITANT — FOSAPREPITANT (FOSAPREPITANT)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2550-2020·2020-07-22

    Access Scientific Recalls Mislabeled Powerwand XL Maximum Barrier Kits

    Access Scientific LLC is recalling 1,710 Powerwand XL kits due to incorrect catheter length labels. The error may cause treatment delays or user annoyance.

    Product
    POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Extended Dwell Catheter made of ChronoFlex C with BioGUARD Technology), Catalog No. 94108, Device UDI 00859821006773/Pacakge UDI 10859821006770 - Product Usage: Introducer with Extended Dwell Catheter is used to gain…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V421000·2020-07-21

    Newmar Recalls Motorhomes with Damaged Rear Power Distribution Modules

    Newmar is recalling specific 2016-2020 motorhomes because a damaged rear Power Distribution Module may cause exterior lights to stop working, increasing crash risk.

    Product
    NEWMAR — NEWMAR NEW AIRE, LONDON AIRE, ESSEX, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V419000·2020-07-20

    2021 Thor Motor Coach motorhomes recalled for battery cable fire risk

    Thor Motor Coach is recalling 2021 motorhomes because an improperly secured battery cable may contact the exhaust manifold and pose a fire risk. Owners should contact Thor Motor Coach for a free inspection and repair.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH QUANTUM, CHATEAU, FREEDOM ELITE, DAYBREAK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V420000·2020-07-20

    Altec Recalls 1995-1998 Aerial Devices Due to Hydraulic Cylinder Defect

    Altec Industries is recalling 1995-1998 A0442 aerial devices because a hydraulic cylinder end gland may fail, causing uncontrolled boom movement and increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V414000·2020-07-17

    Ford Recalls Lincoln MKX and Nautilus for Air Bag Wire Damage Risk

    Ford is recalling 2016-2020 Lincoln vehicles because seat tilt functions may damage air bag wiring, causing unintended deployment or failure to deploy.

    Product
    LINCOLN — LINCOLN MKX, NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V415000·2020-07-17

    Ford Recalls 2020 Escape and Transit Vehicles for Air Bag Defect

    Ford is recalling 2020 Escape and Transit vehicles because a defective air bag component may prevent proper inflation during a crash, increasing injury risk.

    Product
    FORD — FORD ESCAPE, TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V416000·2020-07-17

    Mercedes-Benz Recalls 2019 A 220 Vehicles for Electrical Water Ingress Risk

    Mercedes-Benz is recalling 2019 A 220 vehicles because a poorly installed air conditioning drain hose may allow water to enter electrical components, potentially causing system malfunctions.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ A 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V413000·2020-07-17

    Ford recalls 2021 F-650 and F-750 trucks for missing heat shields

    Ford is recalling certain 2021 F-650 and F-750 trucks because heat-protection components were not installed during assembly. Without these shields, the cabin floor and seat attachments may become too hot and cause burns.

    Product
    FORD — FORD F-650 SD, F-750 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E049000·2020-07-17

    Allison Transmission Drive Units Recalled for Pressure Switch Failure

    Allison Transmission is recalling specific drive units because pressure switches may fail, potentially causing a loss of drive and increasing crash risk.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20150·2020-07-16

    Rocky Mountain Recalls Alloy Instinct and Pipeline Bicycles Due to Frame Cracking

    Rocky Mountain is recalling about 1,530 non-electric alloy frame Instinct and Pipeline bicycles because the front frame triangle can crack, posing fall and injury hazards.

    Product
    Rocky Mountain non-electric alloy frame Instinct, Instinct BC and Pipeline bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20764·2020-07-16

    Polaris Recalls 2015-2020 AXYS Snowmobiles Due to Fire Hazard

    Polaris is recalling approximately 41,200 AXYS snowmobiles because improperly secured fuel hoses may pose a fire hazard. No fires or injuries have been reported.

    Product
    Model Year 2015-2020 AXYS Trail Performance and Crossover snowmobiles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2504-2020·2020-07-15

    CTL Medical Recalls CEZANNE II TLIF Bullet-Tip Cages Due to Fracturing

    CTL Medical Corporation is recalling 46 units of CEZANNE II TLIF Bullet-Tip Cages because reports indicate the devices fractured during insertion.

    Product
    CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H8mm, Part #018.1908.
    Category
    Medical Device
    Distribution
    9 states
  • SevereNHTSA·20V407000·2020-07-15

    Blue Bird Transit Bus Recall for Missing Seat Belt Hardware

    Blue Bird is recalling 2019-2021 Vision and All-American buses because seat belt anchorages may lack reinforcing washers, increasing injury risk in crashes.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS, ALL AMERICAN, VISION, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2501-2020·2020-07-15

    CTL Medical Recalls CEZANNE II TLIF Bullet-Tip Cage Due to Fracturing

    CTL Medical Corporation is recalling 39 units of CEZANNE II TLIF Bullet-Tip Cage because reports indicate the device fractured during insertion.

    Product
    CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L26, H7mm, Part #018.1307.
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Devices)·Z-2489-2020·2020-07-15

    Prodimed Combicath Catheters Recalled for Sterility Assurance Concerns

    Prodimed Plastimed Division is recalling 300 Combicath catheters nationwide due to a lack of assurance of sterility.

    Product
    Prodimed Combicath catheters for blind or fibrescope-guided protected distal bronchial sampling (PDBS)- COMBICATH 90 cm x 1.9 mm Product Code: 58229 19US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2502-2020·2020-07-15

    CTL Medical Recalls CEZANNE II TLIF Bullet-Tip Cage Due to Fracture Reports

    CTL Medical Corporation is recalling 39 units of CEZANNE II TLIF Bullet-Tip Cages because reports indicate the devices fractured during insertion.

    Product
    CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H7mm, Part #018.1907.
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Devices)·Z-2503-2020·2020-07-15

    CTL Medical Recalls CEZANNE II TLIF Bullet-Tip Cage Due to Fracturing

    CTL Medical Corporation is recalling 45 units of CEZANNE II TLIF Bullet-Tip Cages because reports indicate the devices fractured during insertion.

    Product
    CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L26, H8mm, Part #018.1308.
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Devices)·Z-2491-2020·2020-07-15

    Prodimed Combicath Paediatric Catheters Recalled Due to Sterility Assurance Issues

    Prodimed Plastimed Division is recalling 180 units of Combicath Paediatric catheters nationwide because the company cannot assure the sterility of the devices.

    Product
    Prodimed Combicath Paediatric catheters for blind protected distal bronchial sampling- COMBICATH 35 cm x 1.9 mm Product Code: 58 223 19US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1379-2020·2020-07-15

    EMD Serono Recalls Cetrotide Vials Due to Missing Rubber Stoppers

    EMD Serono is recalling 30,756 vials of Cetrotide because missing rubber stoppers could compromise sterility assurance.

    Product
    CETROTIDE — CETROTIDE (CETRORELIX ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V409000·2020-07-15

    Blue Bird Recalls School Buses Due to Seat Belt Anchor Defect

    Blue Bird is recalling 2018-2021 All-American and 2019-2021 Vision school buses because seat belt anchorages may lack reinforcing washers, increasing injury risk in crashes.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide