The Recall Desk

State

Kansas product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52976–53000 of 79649

  • SevereFDA (Devices)·Z-1532-2016·2016-05-11

    B Braun Dialog+ Hemodialysis Machines Recalled for Potential Sensor Leakage

    B Braun Medical Inc. is recalling 40 Dialog+ Hemodialysis machines due to a potential leakage issue with conductivity sensors.

    Product
    Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Product Code 710200K Serial # >202169 and < 203249 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1533-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Machines Due to Sensor Leakage

    B Braun Medical Inc is recalling 318 Dialog+ Hemodialysis machines because conductivity sensors may leak. The recall covers units distributed nationwide.

    Product
    Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL Product Code # 710200S Serial # >200805 and <204001 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V292000·2016-05-11

    Subaru Recalls 2016-2017 Legacy and Outback for Steering Column Defect

    Subaru is recalling 48,819 Legacy and Outback vehicles because an improperly machined steering column may cause loss of steering control, increasing crash risk.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·040-2016·2016-05-11

    Ajinomoto Windsor Recalls Meat and Poultry Products Due to Listeria Risk

    Ajinomoto Windsor is recalling approximately 47 million pounds of not-ready-to-eat meat and poultry products due to possible Listeria monocytogenes contamination.

    Product
    Ajinomoto Windsor Inc. — Ajinomoto Windsor, Inc. Recalls Meat and Poultry Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V285000·2016-05-11

    Forest River Recalls 2016-2017 Berkshire and Cross Country RVs for Sway Bar Defect

    Forest River is recalling specific 2016-2017 Berkshire and 2016 Cross Country recreational vehicles because front sway bar brackets may not fit properly, risking detachment and crashes.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN BERKSHIRE, CROSS COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1606-2016·2016-05-11

    CareFusion Alaris PC Unit Model 8015 Recalled for Power-Up Error

    CareFusion 303, Inc. is recalling 23,397 Alaris PC units, Model 8015, because a super capacitor failure may cause a system error code at power-up.

    Product
    Alaris PC unit, Model 8015 The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1610-2016·2016-05-11

    Applied Medical Recalls Wilson Penile Implantation System Retractor Frame

    Applied Medical Technology Inc is recalling Wilson Penile Implantation System Retractor Frames due to a reported open pouch that breaches sterilization validation.

    Product
    Wilson Penile Implantation System Retractor Frame, Retractor Stays & Penile Elevation Strap, SINGLE USE ONLY Rx ONLY (USA) STERILE EO Do Not Resterilize Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
    Category
    Medical Device
    Distribution
    28 states
  • HighNHTSA·16V286000·2016-05-11

    Great Lakes Drywall Pup Trailers Recalled for Rear Impact Guard Defect

    Great Lakes is recalling 1998-2016 Drywall Pup trailers because rear impact guards do not meet federal safety standards, increasing injury risk in crashes.

    Product
    GREAT LAKES — GREAT LAKES DRYWALL PUP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1598-2016·2016-05-11

    Siemens MAGNETOM MRI Systems Recalled Due to Magnetic Table Cover Hazard

    Siemens is recalling eight MAGNETOM Aera/Skyra MRI systems because the patient table's docking station cover may contain a magnetic plate that attracts to the main magnet.

    Product
    MAGNETOM Aera/Skyra Systems, whole body magnetic resonance imaging systems, Model numbers 10432914, 10432915. Docking station top cover (part no# 10591430) of the removable patient table.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1611-2016·2016-05-11

    Applied Medical Recalls Wilson Implantation System Due to Sterilization Breach

    Applied Medical Technology Inc is recalling 1,100 units of the Wilson Implantation System after a complaint revealed an open pouch that breached sterilization validation.

    Product
    Wilson Implantation System Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Devices)·Z-1609-2016·2016-05-11

    Applied Medical Technology Recalls Self-Retaining Retractor Frames Due to Sterilization Breach

    Applied Medical Technology is recalling 3,754 units of TLC Self-Retaining Retractor Frames because a complaint reported an open pouch, which breaches sterilization validation.

    Product
    TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) STERILE EO Do Not Resterilize. Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Devices)·Z-1608-2016·2016-05-11

    Applied Medical Recalls TLC Self Retaining Retractor Systems Due to Sterilization Breach

    Applied Medical Technology Inc is recalling 5,334 units of TLC Self Retaining Retractor Systems because a complaint reported an open pouch that breaches sterilization validation.

    Product
    TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Devices)·Z-1586-2016·2016-05-11

    Ab Sciex Analyst MD Software Recall for Incorrect Diagnostic Results

    Ab Sciex is recalling Analyst MD software versions 1.6.1 and 1.6.2 because it may display wrong quantitative results, potentially leading to incorrect patient diagnoses.

    Product
    Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the following instruments: API 3200MD" LC/MS/MS System, Instrument Part Number: 5024501; 3200MD QTRAP¿ LC/MS/MS System, Instrument Part Number: 5024500; Triple Quad" 4500MD LC/MS/MS System, Instrument Part Number: 5031257…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1601-2016·2016-05-11

    Siemens Syngo Dynamics PACS Software Recall for Workflow Error

    Siemens is recalling 84 units of Syngo Dynamics software due to a defect that may cause old measurements to be carried forward into new reports.

    Product
    Syngo Dynamics; Kinetdx Picture Archiving and Communications System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V289000·2016-05-11

    Pacific Coachworks Recalls 2016 Rage'N Toy Haulers for Label Error

    Pacific Coachworks is recalling 2016 Rage'N toy haulers because an incorrect Cargo Carrying Capacity value on the Federal Information label could lead to overloading.

    Product
    PACIFIC COACHWORKS — PACIFIC COACHWORKS RAGE'N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16158·2016-05-11

    Bosch Small Angle Grinders Recalled for Overheating and Burn Risk

    Robert Bosch Tool Corp. is recalling about 91,000 Bosch 1380 Slim small angle grinders because they can overheat, melt brush covers, and expose hot components, posing a burn risk.

    Product
    Bosch small angle grinders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1293-2016·2016-05-11

    Emerald Cashew Packs Recalled for Potential Glass Fragments

    Diamond Foods is recalling Emerald 100 Calorie Packs of Cashew Halves & Pieces due to the potential for small glass fragments in the product.

    Product
    Emerald 100 Calorie Packs of Cashew Halves & Pieces, roasted and salted. 7 pack/ 0.62 oz. each (17.5 g). Ingredients: Cashews, Vegetable Oil/Safflower, Sunflower and/or Canola Oil, Salt, Rosemary extract (to preserve freshness: Retail Carton UPC: 0 10300 33324 1; Inner…
    Category
    Food
    Distribution
    23 states
  • ModerateFDA (Food)·F-1166-2016·2016-05-11

    Iowa Select Herbs Recalls Cyperus Leaf for Misbranding and Adulteration

    Iowa Select Herbs LLC is recalling 1-gallon bottles of Alcohol-Free Cyperus Leaf because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.

    Product
    Iowa Select Herbs LLC, Alcohol-Free, Cyperus Leaf, www.iowaselectherbs.com, 1 gallon, Cedar Rapids, IA 52402
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1164-2016·2016-05-11

    Iowa Select Herbs Cranberry Recalled for Misbranding and Adulteration

    Iowa Select Herbs LLC is recalling 7.5 fl. oz. bottles of Cranberry because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.

    Product
    Iowa Select Herbs LLC, Cranberry, www.iowaselectherbs.com, 7.5 fl. Oz., Cedar Rapids, IA 52402
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1197-2016·2016-05-11

    Iowa Select Herbs Recalls Momordica Leaf for Misbranding and Adulteration

    Iowa Select Herbs LLC is recalling Momordica Leaf under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.

    Product
    Iowa Select Herbs LLC, Momordica Leaf, www.iowaselectherbs.com, 1 gallon, Cedar Rapids, IA 52402
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1216-2016·2016-05-11

    Iowa Select Herbs Recalls Rhodiola Root for Misbranding and Adulteration

    Iowa Select Herbs LLC is recalling Rhodiola Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.

    Product
    Iowa Select Herbs LLC, Rhodiola Root, www.iowaselectherbs.com, 1 gallon., Cedar Rapids, IA 52402
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1184-2016·2016-05-11

    Iowa Select Herbs Hawthorn Berry Recalled for Misbranding and Adulteration

    Iowa Select Herbs LLC is recalling Hawthorn Berry dietary supplements because they are misbranded, unapproved new drugs, and adulterated.

    Product
    Iowa Select Herbs LLC, Hawthorn Berry (Crateagus oxycanthus), www.iowaselectherbs.com, 7.5 fl. Oz., Cedar Rapids, IA 52402
    Category
    Food
    Distribution
    Distributed nationwide