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.

50026–50050 of 79646

  • ModerateFDA (Devices)·Z-0136-2017·2016-10-26

    Hand Biomechanics Lab Recalls Agee WristJack Fracture Reduction Systems

    Hand Biomechanics Lab Inc is recalling 65 Agee WristJack Fracture Reduction Systems because a molded beam is slightly larger than optimal, which may make surgical adjustments difficult.

    Product
    Agee-WristJack¿ Fracture Reduction System; Item number: CFD-147. The WristJack Fracture Reduction System is a fracture reduction and external fixation system for treatment of distal radius fractures. This is a single use system used for a trauma related surgery The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0166-2017·2016-10-26

    Entenmann's Little Bites Fudge Brownies Recalled Due to Plastic Presence

    BIMBO Bakeries USA is recalling Entenmann's Little Bites Fudge Brownies because plastic was found in the muffins and brownies.

    Product
    Entenmann's Little Bites Fudge Brownies - 20 muffins, 5 Pouches; Net Wt. 9.75 OZ.; Bimbo Bakeries USA, Inc., Horsham, PA 19044; Best By: October 8, 2016/3098; UPC: 7203001342
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0112-2017·2016-10-26

    Stryker Recalls Sagittal Blades Due to Potential Sterile Barrier Breach

    Stryker Instruments is voluntarily recalling 225 Sagittal Blades due to a potential sterile barrier breach in the packaging.

    Product
    Sagittal Blade 18.0X0.97X90MM, Model Number: 6118-097-090 Product Usage: Heavy duty Sagittal Blades are used to cut bone and bone related tissue in a variety of orthopedic procedures. Typical procedures include, total-knee, uni-compartmental knee, hip, shoulder and ankle…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0092-2017·2016-10-26

    Ortho VITROS URIC Slides Recalled Due to NAC Interference

    Ortho-Clinical Diagnostics is recalling VITROS URIC Slides because N-Acetylcysteine (NAC) can interfere with the assay results.

    Product
    VITROS Chemistry Products URIC Slides, REF/Product Code 194 3927 (300 slides per sales unit), Unique Device Identifier No. 10758750000340, Rx ONLY, IVD --- For in vitro diagnostic use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0128-2017·2016-10-26

    BD Biosciences Recalls Contaminated CD79b PE Antibody Reagent

    Becton, Dickinson and Company is recalling 14 units of CD79b PE antibody reagent due to contamination with a FITC conjugate of unknown specificity.

    Product
    CD79b PE (ASR) , Catalog number 335816 ; Hematology: The CD79b antibody recognizes an epitope on the extracellular domain of a 3640 kilodalton (kDa) type I membrane glycoprotein. Immunoglobulin (Ig) antigen receptors are composed of a non-covalently associated complex of Ig…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0130-2017·2016-10-26

    ConMed Recalls CORE Suction Irrigation Handpieces Due to Packaging Seal Defects

    ConMed Corporation is recalling CORE Suction Irrigation Handpieces because packaging seal creases may compromise sterility. The recall covers units distributed in the US and internationally.

    Product
    CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single Solution or Dual Bags, Catalog Number CD8190 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0089-2017·2016-10-26

    Ortho VITROS Chemistry GLU Slides Recalled for Potential Assay Interference

    Ortho-Clinical Diagnostics is recalling VITROS GLU Slides because certain substances, including N-Acetylcysteine, may interfere with glucose measurements.

    Product
    VITROS Chemistry Products GLU Slides, REF/Product Code 170 7801 (300 slides per sales unit), Unique Device Identifier No. 10758750009572, Rx ONLY, IVD --- For in vitro diagnostic use only. VITROS Chemistry Products GLU Slides quantitatively measure glucose (GLU)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0226-2017·2016-10-26

    Hillcrest Farms Poultry Gravy Mix Recalled for Lead Contamination

    National Foods Packaging Inc is recalling Hillcrest Farms Poultry Gravy Mix because a spice ingredient was found to contain elevated levels of lead.

    Product
    Hillcrest Farms Poultry Gravy Mix in 25lb brown poly-lined bags
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0165-2017·2016-10-26

    Entenmann's Little Bites Variety Recalled Due to Plastic Presence

    BIMBO Bakeries USA Inc. is recalling 45,600 boxes of Entenmann's Little Bites Variety due to the presence of plastic in the muffins and brownies.

    Product
    Entenmann's Little Bites Variety - 20 pouches labeled for resale 10 Chocolate Chip; 5 Blueberry; 5 Fudge Brownie; Net Wt 2 lbs.; Distributed by: Entenmann's Inc., General Offices, PO #976, Horsham, PA 19044. Best by: September 24, 2016/ 3098; UPC:7203001799
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0111-2017·2016-10-26

    Teva Recalls Paricalcitol Capsules Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling specific lots of Paricalcitol Capsules because stability testing revealed out-of-specification impurities.

    Product
    PARICALCITOL Capsules, 4 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7658-56.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0110-2017·2016-10-26

    Teva Recalls Paricalcitol Capsules Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling 5,556 bottles of Paricalcitol Capsules because stability testing revealed out-of-specification impurities.

    Product
    PARICALCITOL Capsules, 2 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7657-56.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0109-2017·2016-10-26

    Teva Recalls Paricalcitol Capsules Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling 32,015 bottles of Paricalcitol Capsules, 1 mcg, because stability testing revealed out-of-specification impurities.

    Product
    PARICALCITOL Capsules, 1 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7656-56.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E079000·2016-10-25

    Atwood Recalls Left Side Seat Adjusters for Crash Safety Non-Compliance

    Atwood Mobile Products is recalling specific left side seat adjusters used in vehicle seat belts because they may allow seats to move during a crash, increasing injury risk.

    Product
    SEAT BELTS:FRONT:ANCHORAGE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·100-2016·2016-10-25

    Crider Recalls Canned Organic Roasted Chicken Breast Due to Foreign Matter

    Crider Inc. is recalling approximately 5,610 pounds of canned Organic Roasted Chicken Breast due to possible foreign matter contamination.

    Product
    Crider, Inc. — Crider Inc. Recalls Canned Organic Roasted Chicken Breast Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16E080000·2016-10-25

    Ivolution Recalls JX-SKY Helmets Due to Crash Safety Non-Compliance

    Ivolution Sports is recalling specific JX-SKY helmets because a metal screw prevents a detachable feature from releasing during a crash, increasing neck injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V772000·2016-10-24

    Jayco Recalls 2017 Eagle Fifth Wheel Trailers for Axle Defect

    Jayco is recalling specific 2017 Eagle fifth wheel trailers due to axles with insufficient load capacity, which may lead to tire failure and increased crash risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V769000·2016-10-24

    ARBOC Spirit of Liberty Recall for Engine Run Lockout Wiring Defect

    ARBOC is recalling 2016 Spirit of Liberty vehicles because improper wiring may allow the engine to start while a mechanic is working on it, posing a risk of injury or death.

    Product
    ARBOC — ARBOC SPIRIT OF LIBERTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V775000·2016-10-24

    Toyota Recalls 2016 Highlanders Due to Brake Fluid Sensor Wiring Issue

    Toyota is recalling 7,056 model year 2016 Highlanders because the brake fluid level sensor may not be connected to the wire harness, potentially decreasing braking performance.

    Product
    TOYOTA — TOYOTA HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V765000·2016-10-21

    Navistar Recalls School Buses with Defective Wheelchair Lifts

    Navistar is recalling certain 2015-2017 IC Bus school buses equipped with specific Ricon wheelchair lifts. The defect may cause the lift platform to fall out of the vehicle, increasing injury risk.

    Product
    IC BUS — IC BUS CESB, RESB, CASB, AE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V764000·2016-10-21

    Kaufman Recalls 2015-2016 Mini Car Haulers Due to Spring Defect

    Kaufman is recalling 2015-2016 Mini Car Haulers because a spring eye may break, allowing the axle to slide and potentially causing a crash.

    Product
    KAUFMAN — KAUFMAN MINI CAR HAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide