The Recall Desk

State

Kansas product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42176–42200 of 79631

  • HighFDA (Devices)·Z-1438-2018·2018-04-25

    Philips T5-NT MRI Scanner Recalled for Helium Gas Risk

    Philips is recalling 8,205 T5-NT MRI scanners worldwide due to a potential risk of helium gas release in the examination room during a magnet quench.

    Product
    T5-NT, Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1024-2018·2018-04-25

    Mrs. Gerry's Egg Salad Recalled for Undeclared Imitation Crab Meat

    Mrs. Gerry's Kitchen is recalling 5 lb. Egg Salad products because they may contain undeclared traces of imitation crab meat.

    Product
    Mrs. Gerry's Egg Salad, Net Wt. 5 lb. (2.26kg), UPC 17839-60605. Keep Refrigerated. Manufactured by Mrs. Gerry's, Albert Lea, MN 56007
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1413-2018·2018-04-25

    Philips Brilliance 64 CT System Recalled for Emergency Stop Defect

    Philips Medical Systems is recalling six Brilliance 64 CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.

    Product
    Brilliance 64 - Model no. 728231, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1433-2018·2018-04-25

    Philips Intera 1.5T MRI Systems Recalled for Helium Gas Risk

    Philips is recalling Intera 1.5T MRI systems due to a potential risk of helium gas release during a magnet quench.

    Product
    Intera 1.5T; 1) Intera 1.5T Omni/Stellar Model 781104, 2) Intera 1.5T Power/Pulsar Model 781105, 3) Intera 1.5T Master/Nova Model 781106, 4) Intera 1.5T Master CV Model 781107, 5) Intera 1.5T Explorer/ Nova Dual Model 781108, 6) Intera 1.5T IT Model 781160, 7) Intera 1.5T…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1378-2018·2018-04-25

    Cook Inc. Recalls MINC Benchtop Incubators Due to Temperature Control Defect

    Cook Inc. is recalling 4,451 MINC Benchtop Incubators because a heater defect may cause temperatures to become too high or too low for proper cell culture.

    Product
    MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a microprocessor controlled, gassed, humidified, incubator intended for use in cell culture.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1414-2018·2018-04-25

    Philips IQon Spectral CT Recalled for Emergency Stop Defect

    Philips is recalling 47 IQon Spectral CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.

    Product
    IQon Spectral CT - Model no. 728332, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1107-2018·2018-04-25

    Hungry Jack Pancake and Waffle Mix Recalled for Salmonella

    The J.M. Smucker Company is recalling Hungry Jack Original Pancake & Waffle Mix because the product tested positive for salmonella.

    Product
    HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-1401-2018·2018-04-25

    Siemens Oncor Impression Plus Linear Accelerator Software Recall

    Siemens is recalling 15 Oncor Impression Plus linear accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    ONCOR Impression Plus, Digital Linear Accelerator, Model No. 05857912 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1389-2018·2018-04-25

    Stryker Power-LOAD Cot Fastening System Recalled for Broken Floor Plates

    Stryker is recalling 4,724 Power-LOAD Cot Fastening Systems because the floor plates holding ambulance cot anchors may be broken.

    Product
    Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000, UDI: 07613327261523 Power-LOAD is intended to assist with loading and unloading of a compatible wheeled stretcher (ambulance cot) to and from a transport vehicle and to secure the ambulance cot during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1410-2018·2018-04-25

    Philips CT Scanner Recall Due to Emergency Stop Defect

    Philips is recalling 106 Brilliance Big Bore CT scanners because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading or unloading.

    Product
    Brilliance Big Bore (Oncology) - Model no. 728243, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1030-2018·2018-04-25

    Festival Foods Potato Salad Recalled for Undeclared Imitation Crab Meat

    Mrs Gerry's Kitchen is recalling Festival Foods Potato Salad because it may contain undeclared traces of imitation crab meat.

    Product
    Festival Foods Potato Salad packaged in the following size containers: Net Wt. 6 oz. (170g), UPC 17839-22388, Net Wt. 1 lb. (454 g) UPC 17839-22301, Net Wt. 3 lb. (1.36 kg), UPC 17839-22303. Net Wt. 35 lb. 15.87 kg), UPC 17839-22335. Keep Refrigerated. Made for…
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1402-2018·2018-04-25

    Siemens PRIMUS HI Digital Linear Accelerator Software Recall

    Siemens is recalling 18 PRIMUS HI Digital Linear Accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    PRIMUS HI, Digital Linear Accelerator, Model No. 04504200 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1431-2018·2018-04-25

    Philips Intera 0.5T MRI Recalled for Helium Gas Risk

    Philips is recalling 8,205 Intera 0.5T MRI scanners worldwide due to a potential risk of helium gas release during a magnet quench.

    Product
    Intera 0.5T Standard, Model 781101 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1406-2018·2018-04-25

    Philips Ingenuity Core CT Systems Recalled for Couch Movement Hazard

    Philips is recalling 281 Ingenuity Core CT systems because the emergency stop may fail to lock the couch, allowing it to move during patient loading.

    Product
    Ingenuity Core - Model no. 728321, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1381-2018·2018-04-25

    Zimmer Biomet Recalls Segmental System Proximal Femoral Components

    Zimmer Biomet is recalling specific proximal femoral components due to potential machining debris that may not have been adequately removed during cleaning.

    Product
    Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is used for solving complex salvage cases to address patients with severe bone loss associated with disease, trauma, or revision.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1397-2018·2018-04-25

    Siemens MEVATRON M2 Linear Accelerator Recalled for Collision Risk

    Siemens is recalling 18 MEVATRON M2 linear accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1442-2018·2018-04-25

    Philips T5 MRI Scanner Recalled for Helium Gas Risk

    Philips is recalling T5 MRI scanners due to a potential risk of helium gas release during a magnet quench.

    Product
    T5 Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1428-2018·2018-04-25

    Halyard Closed Suction System Flex Connectors May Disconnect During Use

    Halyard Health is recalling certain Closed Suction Systems because Flex Connectors may become loose or disconnect before or during use.

    Product
    Halyard Closed Suction System for Adults, Turbo- cleaning¿Closed¿Suction¿System¿for¿Adults,¿Double¿Swivel¿Elbow (DSE). Used to aspirate liquids or semisolids from a patient's upper airway. a. HALYARD* TURBO-CLEANING 14FR DSE 21.3IN/54 CM (GREEN); b. HALYARD* TRACH…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18739·2018-04-25

    HD Supply Recalls Seasons Ceiling Fans Due to Impact Hazard

    HD Supply is recalling Seasons ceiling fans because brackets can break, causing blades to fall. No injuries have been reported, but one instance of minor property damage occurred.

    Product
    Seasons ceiling fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1400-2018·2018-04-25

    Siemens ONCOR Impression Linear Accelerator Software Update Recall

    Siemens is recalling seven ONCOR Impression Digital Linear Accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    ONCOR Impression , Digital Linear Accelerator, Model No. 05857920 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1435-2018·2018-04-25

    Philips Achieva 1.5T MRI Systems Recalled for Helium Gas Risk

    Philips is recalling 8,205 Achieva 1.5T MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.

    Product
    Achieva 1.5T: 1) Nova (Dual), Model 781173, 2) Achieva 1.5T Initial Systems Model 781178, 3) Achieva 1.5T Nova Model 781196, 4) Achieva 1.5T Conversion Model 781283, 5) Achieva 1.5T Model 781296, 6) Achieva 1.5T R5 based Model 781343, 7) Achieva 1.5T Conversion R5 based Model…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1439-2018·2018-04-25

    Philips ACS-NT MRI Scanner Recalled for Helium Gas Leak Risk

    Philips is recalling 8,205 ACS-NT MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.

    Product
    ACS-NT, Model 78108 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1403-2018·2018-04-25

    Teleflex Medical One Way Valve Recall for Potential Disconnection

    Teleflex Medical is recalling specific lots of HUDSON RCI One Way Valves because they may disconnect, causing an interruption of ventilation to patients.

    Product
    Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in respiratory and anesthesia circuits to connect two or more components of a breathing system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1408-2018·2018-04-25

    Philips Brilliance iCT CT Systems Recalled for Emergency Stop Defect

    Philips is recalling 295 Brilliance iCT CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading.

    Product
    Brilliance iCT - Model no. 728306 Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1031-2018·2018-04-25

    Mrs. Gerry's Potato Salad Recalled for Undeclared Imitation Crab Meat

    Mrs. Gerry's is recalling 12 lb. potato salad for undeclared imitation crab meat. Consumers with shellfish allergies should not eat the product.

    Product
    Mrs. Gerry's Knowlan's Homestyle Potato Salad Net Wt. 12 lbs. (5.44 kg), UPC 17839-22912. Keep Refrigerated. Manufactured by Mrs. Gerry's, Albert Lea, MN 56007
    Category
    Food
    Distribution
    12 states