The Recall Desk

State

Kansas product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39001–39025 of 79628

  • ModerateFDA (Devices)·Z-0392-2019·2018-11-14

    Ortho-Clinical Diagnostics Recalls VITROS Vitamin B12 Reagent Packs

    Ortho-Clinical Diagnostics is recalling VITROS Vitamin B12 Reagent Packs due to a potential for increased calibration failures.

    Product
    VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only For the quantitative measurement of vitamin B12 in human serum and plasma (EDTA or heparin) using the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0383-2019·2018-11-14

    Qiagen EZ1 Advanced XL Recalled for Potential Heater Malfunction

    Qiagen is recalling 298 EZ1 Advanced XL instruments due to a power board defect that may cause heater malfunctions and compromise nucleic acid extractions.

    Product
    EZ1 Advanced XL, Model Number: 9001492, GTIN: 04053228010760 Product Usage: The EZ1 Advanced XL is designed to perform automated isolation and purification of nucleic acids. It is intended to be used only in combination with QIAGEN kits indicated for use with the EZ1…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0385-2019·2018-11-14

    CareFusion Recalls Alaris Infusion Pump Administration Sets Due to Priming Issues

    CareFusion 303, Inc. is recalling Alaris Infusion Pump administration sets because users reported being unable to prime the devices.

    Product
    Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris Pump Module/Medley Pump Module/Gemini Infusion Pump, REF 10011301, CareFusion, WARNING: TO PREVENT FREE-FLOW, CLOSE SET CLAMP WHEN SAFETY CLAMP FITMENT ON PUMP SEGMENT IS OPEN, Fluid path is STERILE and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0217-2019·2018-11-14

    Janssen Recalls Ortho-Novum 1/35 Due to Incorrect Dispenser Instructions

    Janssen Pharmaceuticals is recalling Ortho-Novum 1/35 tablets because the packaging included instructions for the wrong type of pill dispenser.

    Product
    Ortho-Novum 1/35 (norethindrone/ethinyl estradiol) Tablets, 1 mg/0.035 mg, 28-Day Regimen per pouch (NDC 50458-176-28), 6 Veridate Tablet Dispensers and 6 refills per carton (NDC 50458-176-06), Rx only, Manufactured by: Janssen Ortho, LLC, Manati, Puerto Rico 00674; Manufactured…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0223-2019·2018-11-14

    Tailor Made Compounding Recalls Tesamorelin Vials Due to Incorrect Expiration Dates

    Tailor Made Compounding is recalling 10,280 vials of Tesamorelin because the labels indicate a 1-year expiration date instead of the correct 6-month date.

    Product
    Tesamorelin, 1mg/vial, 6mL vial, Lyophilized Powder for Reconstitution and Subcutaneous Injection, Rx Only, Tailor Made Compounding, Nicholasville, KY 40356
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0404-2019·2018-11-14

    Medtronic Navigation 0-arm 02 Imaging System Software and Hardware Recall

    Medtronic Navigation is recalling 641 O-arm 02 Imaging Systems to correct software version 4.1.0, update manuals and labels, and replace blown fuses in the AC power input circuit.

    Product
    Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic x-ray system: OARM BI70002000 SYS IMAGING 02 Model: BI70002000 OARM BI70002000R SYS IMAGING 02 REFURB Model: BI70002000R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0377-2019·2018-11-14

    AROA Endoform Dermal Template Recalled for Potential Pouch Seal Failure

    AROA Biosurgery is recalling Endoform Dermal Template 2x2 units due to a potential for pouch seal failure.

    Product
    Endoform Dermal Template 2x2, SKU 529311 Product Usage: Endoform Dermal Template is a sterile, single use ovine forestomach derived extracellular matrix intended to cover, protect and provide a moist wound environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0247-2019·2018-11-14

    Medline Recalls SparkleFresh Toothpaste Due to Microbial Contamination

    Medline Industries is recalling SparkleFresh fluoride toothpaste nationwide due to microbial contamination of the non-sterile product.

    Product
    SPARKLEFRESH — SPARKLEFRESH (SODIUM MONOFLUOROPHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0405-2019·2018-11-14

    Integrity Implants Recalls FlareHawk Interbody Fusion System Instructions for Use

    Integrity Implants is correcting Instructions for Use for the FlareHawk Interbody Fusion System due to discrepancies in cleaning parameters.

    Product
    FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product Usage: Indicated for spinal intervertebral body fusion with autogenous bone graft in skeletally mature individuals with degenerative disc disease.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0389-2019·2018-11-14

    Medtest AutoHDL/LDL Cholesterol Calibrator Recalled for Missing Vial Labels

    Medtest Holdings is recalling 22 vials of AutoHDL/LDL Cholesterol Calibrator shipped without labels in five states.

    Product
    Pointe Scientific AutoHDL/LDL Cholesterol Calibrator, Catalog Number H7545-CAL - Product Usage: For the calibration of Pointe Scientific s autoHDL and autoLDL Cholesterol Reagent Set in serum or plasma. For in vitro diagnostic use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19715·2018-11-13

    YTL International Recalls County Line Log Splitters Due to Injury Hazard

    YTL International is recalling about 1,460 County Line log splitters because welding on the tongue box assembly can crack, causing the tank to disconnect and posing an injury hazard.

    Product
    County Line log splitters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V800000·2018-11-13

    Volvo Recalls 2017-2019 Models Due to Telematics Software Error

    Volvo is recalling 2017-2019 models because a software error may prevent GPS location data from reaching emergency personnel during a crash.

    Product
    VOLVO — VOLVO XC90, V60, S90, XC60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V796000·2018-11-12

    Coach and Equipment Recalls 2015-2018 Phoenix and Metro Lite Buses

    Coach and Equipment is recalling 864 transit buses because foldaway seats may not lock properly, increasing injury risk in crashes.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX, METRO LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V798000·2018-11-12

    Champion and Goshen Transit Buses Recalled for Seat Lock Defect

    Champion Bus is recalling 2017-2018 transit buses because foldaway seats may not stay locked during a crash or sudden stop, increasing injury risk.

    Product
    CHAMPION — CHAMPION, GOSHEN LF TRANSPORT, CHALLENGER, G-FORCE, IMPULSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V799000·2018-11-12

    Starcraft Transit Bus Recall for Foldaway Seat Locking Defect

    Forest River is recalling specific Starcraft transit buses because foldaway seat cushions may not stay locked in a crash, increasing injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, STARCRAFT SENATOR II, ALLSTAR, STARLITE, STARQUEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V792000·2018-11-09

    Altec Recalls 2017-2018 Aerial Devices Due to Wiring Fire Risk

    Altec is recalling 186 aerial devices from 2017-2018 because under-hood wiring may be damaged by sharp edges, increasing the risk of a fire.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V794000·2018-11-09

    Terex Recalls 2017-2018 Digger Derrick Vehicles Due to Weld Defect

    Terex is recalling 2017-2018 Digger Derrick vehicles because insufficient welds on the guide bar may cause the guide arm to fall, posing an injury risk to nearby personnel.

    Product
    TEREX — TEREX DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V788000·2018-11-09

    Eldorado National Recalls 2014-2018 Vans Due to Seat Lock Defect

    Eldorado National is recalling 2014-2018 Aerolite, Aerotech, Impulse, and World Trans vans because foldaway seats may not stay locked during a crash, increasing injury risk.

    Product
    GOSHEN — GOSHEN, ELDORADO IMPULSE, AEROLITE, AEROTECH, WORLD TRANS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V791000·2018-11-09

    Altec Cranes and Digger Derricks Recalled for Wiring Fire Risk

    Altec is recalling 2008-2018 cranes and digger derricks because undersized wiring may overheat and cause a fire. Owners should contact Altec for a free repair.

    Product
    ALTEC — ALTEC CRANE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V790000·2018-11-09

    Keystone Recalls 2018-2019 Raptor Trailers Due to Tire Rubbing

    Keystone is recalling 2018-2019 Raptor recreational trailers because tires may rub against the frame, potentially affecting handling and increasing crash risk.

    Product
    KEYSTONE — KEYSTONE RAPTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19029·2018-11-08

    A. O. Smith Recalls Ultra-Low NOx Water Heaters Due to Fire Hazard

    A. O. Smith is recalling approximately 616,000 gas water heaters because a torn burner screen can cause excess heat and fire if installed on combustible floors.

    Product
    Ultra-Low NOx water heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide