The Recall Desk

State

Kansas product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31876–31900 of 79558

  • ModerateFDA (Devices)·Z-1486-2020·2020-03-25

    Philips Allura Exper FD Series X-Ray Generator Recall

    Philips is recalling Allura Exper FD Series X-ray generators because a capacitor may fail after electrical surges, preventing image acquisition.

    Product
    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1496-2020·2020-03-25

    Siemens Artis Q.zen Angiography Systems Recalled for Software Movement Issue

    Siemens is recalling Artis Q.zen angiography systems because a software issue could block stand and table movements.

    Product
    Artis Q.zen Biplane, Model No. 10848355 Artis Q.zen Ceiling, Model No. 10848354 Artis Q.zen Floor, Model No. 10848353 Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1044-2020·2020-03-25

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Therapeutics is recalling Daytrana (methylphenidate) patches because the delivery system failed mechanical peel and shear specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1043-2020·2020-03-25

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed mechanical peel and shear specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1051-2020·2020-03-25

    Breckenridge Recalls Solifenacin Succinate Tablets Due to Manufacturing Deviations

    Breckenridge Pharmaceutical is recalling specific lots of Solifenacin Succinate Tablets because manufacturing deviations may have resulted in the production of Solifenacin Tartrate.

    Product
    Solifenacin Succinate Tablets, 10 mg, packaged in a) 30-count bottles (NDC 51991-894-33) and b) 90-count bottles (NDC 51991-894-90), Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487; Manufactured by: Piramal Enterprises Limited Plot No 67-70, Sector -2…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1494-2020·2020-03-25

    Philips Allura Centron X-ray System Recalled for Capacitor Failure

    Philips is recalling 87 Allura Centron X-ray systems because a capacitor may fail after electrical surges, preventing image acquisition.

    Product
    Cardio Vascular-Allura Centron, system code 722400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1042-2020·2020-03-25

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Therapeutics is recalling Daytrana (methylphenidate) patches because the delivery system failed mechanical peel and shear specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1493-2020·2020-03-25

    Philips Allura CV20 X-ray System Recalled for Capacitor Failure

    Philips is recalling 128 Allura CV20 X-ray systems because a capacitor may fail after electrical surges, preventing image acquisition.

    Product
    Allura CV20, system code 722031
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1050-2020·2020-03-25

    Breckenridge Recalls Solifenacin Succinate Tablets Due to Manufacturing Deviations

    Breckenridge Pharmaceutical is recalling specific lots of Solifenacin Succinate Tablets because manufacturing deviations may have resulted in the product converting to Solifenacin Tartrate.

    Product
    Solifenacin Succinate Tablets, 5mg, packaged in a) 30-count bottles (NDC 51991-893-33) and b) 90-count bottles (NDC 51991-893-90) Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487; Manufactured by: Piramal Enterprises Limited Plot No 67-70, Sector -2…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1058-2020·2020-03-25

    Jubilant Cadista Recalls Pantoprazole Sodium Tablets Due to CGMP Deviations

    Jubilant Cadista Pharmaceuticals is recalling 89,376 bottles of Pantoprazole Sodium Delayed-Release Tablets due to dark brown discoloration on tablet edges.

    Product
    Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg, 90 count bottle, Rx Only, Manufactured by Jubilant Generics Ltd, Roorkee-247661 India, NDC 59746-284-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0839-2020·2020-03-25

    Outshine Fruit Bars Recalled Due to White Plastic Pieces

    Dreyers Grand Ice Cream is recalling Outshine Fruit Bars because consumers reported finding pieces of white plastic in the product.

    Product
    Outshine Fruit Bars - Variety Pack (contains 24 x 5 oz. units) Strawberry, Pineapple, Grape, Tangerine Repack UPC: 041548816678
    Category
    Food
    Distribution
    39 states
  • ModerateFDA (Devices)·Z-1487-2020·2020-03-25

    Philips Integris Allura X-ray Systems Recalled for Capacitor Failure

    Philips is recalling 70 Integris Allura 15 & 12 X-ray systems because a capacitor may fail, preventing image acquisition.

    Product
    Integris Allura 15 & 12, monoplane (system code 722043) and biplane (system code 722044)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1032-2020·2020-03-25

    Sun Pharmaceutical Recalls Doxycycline Capsules Due to Manufacturing Deviations

    Sun Pharmaceutical Industries is recalling 624 bottles of Doxycycline Capsules, 75 mg, because they were not manufactured under Current Good Manufacturing Practice conditions.

    Product
    DOXYCYCLINE — DOXYCYCLINE (DOXYCYCLINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1045-2020·2020-03-25

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed mechanical peel and shear specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1029-2020·2020-03-25

    Strides Pharma Recalls Potassium Chloride Tablets Due to Oversized Size

    Strides Pharma Science Limited is recalling specific lots of Potassium Chloride Extended-Release Tablets because oversized tablets were found.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V175000·2020-03-23

    2021 Ford E-350 and E-450 wire harness may damage fuel pump and ABS

    Ford is recalling 2021 E-350 and E-450 vehicles because a rear wire harness may contact the frame and damage circuits for the fuel pump and anti-lock braking system, potentially causing engine stall or loss of braking control.

    Product
    FORD — FORD E-450, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V176000·2020-03-23

    Freightliner Trucks Recalled for Axle Lubrication Defect

    Daimler Trucks is recalling 2019-2020 Freightliner M2 and 108SD trucks because insufficient axle lubrication may damage wheel bearings, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V177000·2020-03-23

    Ford Recalls 2014-2016 Vehicles for Door Latch Defect

    Ford is recalling 2014-2016 Fiesta, Fusion, and Lincoln MKZ vehicles because a door latch component may break, causing doors to open while driving.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION, FIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V168000·2020-03-20

    Terex Recalls 2009-2016 Aerial Devices Due to Lift Cylinder Defect

    Terex is recalling 2009-2016 TCX and SML aerial devices because lift cylinder rod eyes may fail, causing the boom to drift down and increasing injury risk.

    Product
    TEREX — TEREX TCX, SML
    Category
    Vehicle
    Distribution
    Distributed nationwide