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.

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.

48251–48275 of 79646

  • SevereFDA (Devices)·Z-1185-2017·2017-02-15

    Invacare Bariatric Bed Junction Box Recalled for Fire Risk

    Invacare is recalling 161 bariatric bed junction boxes due to a quality issue that may cause sparks and result in a fire.

    Product
    Junction Box - 1104343 and 1193560
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1182-2017·2017-02-15

    Invacare Bariatric Bed Recall Due to Fire Hazard

    Invacare is recalling 411 bariatric beds because the junction box may emit sparks and cause a fire.

    Product
    Bariatric Bed - BAR600IVC
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Food)·F-1435-2017·2017-02-15

    Dutch Valley Recalls Cappuccino Snack Mix Due to Salmonella Risk

    Dutch Valley Food Distributors is recalling Cappuccino Snack Mix because it may be contaminated with Salmonella. The recall affects 157 cases distributed across 22 states.

    Product
    Cappuccino Snack Mix Lot code: 20161027; Best By: 05/25/17 Net Wt: 10 lb (2-5lb bags)
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-1184-2017·2017-02-15

    Invacare Recalls Bariatric Bed Foot Sections Due to Fire Risk

    Invacare Corporation is recalling 292 bariatric bed foot sections because a quality issue with the junction box may cause sparks and result in a fire.

    Product
    Foot Section - BAR5490IVC
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Food)·F-1447-2017·2017-02-15

    Circle U Foods Recalls Taco Seasoning for Potential Glass Inclusion

    Circle U Foods, Inc. is recalling 8 cases of 1.1250 lb Taco Seasoning bags due to a potential glass inclusion. The product was distributed in Texas, Illinois, Kansas, and North Carolina.

    Product
    Circle U Foods, Inc. Product Code: 100002 AF/TV Taco Seasoning Bag Weight: 1.1250 Lbs.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1448-2017·2017-02-15

    Circle U Foods Recalls Cajun Buttermilk Dressing Due to Glass Inclusion

    Circle U Foods is recalling 29 cases of Cajun Buttermilk Dressing due to potential glass inclusion. The product was distributed in Texas, Illinois, Kansas, and North Carolina.

    Product
    Circle U Foods, Inc. Product Code: 908041 RCC/Cajun Buttermilk Dressing Bag Weight: 0.88 Lbs.
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·17V102000·2017-02-15

    Prevost Recalls 2017 Motor Coaches Due to Steering Arm Lever Defect

    Prevost is recalling 2017 H3-45 and X3-45 motor coaches because incorrectly forged steering arm levers may crack and fail, increasing crash risk.

    Product
    PREVOST — PREVOST H3-45, X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1138-2017·2017-02-15

    Carestream DRX-Revolution Mobile X-Ray System Recalled for Brake Failure

    Carestream Health is recalling DRX-Revolution Mobile X-Ray Systems because a complaint alleged the unit could not be stopped when applying the brake, resulting in a crash into an elevator.

    Product
    Carestream DRX-Revolution Mobile X-Ray System, Model DRXR-1, Catalog No. 1019397 (all other countries), Catalog No. 1060177 (China only) -- Carestream Health, Inc. 150 Verona Street, Rochester, NY 14608
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1439-2017·2017-02-15

    Subco Pistachio Pudding Recalled for Possible Salmonella in Milk Ingredient

    Subco Foods is recalling Best Choice Pistachio Instant Pudding & Pie Filling because a milk powder ingredient may be contaminated with Salmonella.

    Product
    Best Choice Pistachio Instant Pudding & Pie Filling, UPC 0 70038 31220 8, 3.4 oz, Distributed by Associated Wholesale Grocers, INC.
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-1438-2017·2017-02-15

    Subco Recalls Lemon Pudding for Possible Salmonella in Milk Ingredient

    Subco Foods of Wisconsin is recalling Best Choice and Always Save Lemon Instant Pudding & Pie Filling because a milk ingredient may contain Salmonella.

    Product
    Best Choice Lemon Instant Pudding & Pie Filling UPC 0 70038 31222 2, 3.4 oz, Distributed by Associated Wholesale Grocers, INC, and Always Save Lemon Instant Pudding & Pie Filling; UPC 0 70038 31215 4, 3.4 oz,. Distributed by Associated Wholesale Grocers, INC .
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-1436-2017·2017-02-15

    Subco Foods Recalls Vanilla Pudding Due to Salmonella Risk

    Subco Foods of Wisconsin is recalling specific vanilla pudding products because an ingredient, high heat nonfat dry milk powder, may be contaminated with Salmonella.

    Product
    Bakers Corner Vanilla Instant Pudding & Pie Filling, UPC 0 41498 15253 6 Distributed by ALDI; Best Choice Vanilla pudding UPC 0 70038 31218 5 Distributed by Associated Wholesale Grocers, INC(AWG) and Always Save Vanilla Pudding, UPC 0 70038 31200 0, Distributed by Associated…
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-1137-2017·2017-02-15

    AngioDynamics Recalls Celerity ECG Cable Accessory Packs Due to Soldering Defect

    AngioDynamics is recalling Celerity ECG Cable Accessory Packs because the ECG clip cable may not be soldered correctly, potentially preventing the device from conducting ECG signals.

    Product
    Celerity ECG Cable Accessory Pack, STERILE, Rx ONLY - distributed under the following labels: (a) angiodynamics UPN/Product No. H787471431, REF/Catalog No. 47-143 -- Legal Manufacturer: AngioDynamics, Inc. 10 Glens Falls Technical Park, Glens Falls, NY 12801; and (b) medCOMP…
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Devices)·Z-0927-2017·2017-02-15

    Bayer Recalls Medrad Intego PET Infusion System Pumps

    Bayer is recalling Medrad Intego PET Infusion System pumps because the administration sets may produce particulates in radiopharmaceutical vials.

    Product
    MEDRAD Intego PET Infusion System - Pump Intended to deliver accurate doses of Fluoredeoxyglucose or F-Sodium Fluoride and commonly used flushing solutions to patients during molecular imaging (nuclear medicine) diagnostic procedures. It is also intended to provide effective…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1449-2017·2017-02-15

    Circle U Foods Recalls Bayou Seasoning Due to Potential Glass Inclusion

    Circle U Foods, Inc. is recalling 8 cases of Razzoo's/Bayou Seasoning due to a potential glass inclusion hazard.

    Product
    Circle U Foods, Inc. Product Code: 900012 Razzoo's/Bayou Seasoning, RCC/Bayou Seasoning Bag Weight: 0.29 Lbs.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1178-2017·2017-02-15

    Boston Scientific Recalls EMBLEM S-ICD Programmer Model 3200

    Boston Scientific is recalling 4,500 EMBLEM S-ICD Programmer Model 3200 units due to a potential risk of radio frequency interference causing unintended commands during in-clinic sessions.

    Product
    Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1144-2017·2017-02-15

    Physio-Control Recalls LIFEPAK 15 Defibrillators with Erroneous CO2 Readings

    Physio-Control is recalling LIFEPAK 15 Monitor/Defibrillators with End-Tidal CO2 options because the CO2 reading may intermittently display an incorrect value of XXX.

    Product
    LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1149-2017·2017-02-15

    Stryker Leibinger Recalls Surgical Drainage Accessories Due to Sterility Labeling Error

    Stryker Leibinger is recalling QUINTUBE Monitor Packs and SPG Bulb Drain Systems because non-sterile products were incorrectly labeled as sterile.

    Product
    QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Flat w/Center Holes (Sterile) Accessories to TLS Surgical Drainage System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1142-2017·2017-02-15

    Merge Healthcare Recalls Eye Station Imaging Devices Due to Capture Failures

    Merge Healthcare is recalling 182 Eye Station capture stations because they may fail to capture eye images as intended, posing a risk to patient health.

    Product
    Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager distributed by Ophthalmic Imaging Systems (OIS). Model number 136 T1700 Capture Stations & 46 T5810 Capture Stations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1148-2017·2017-02-15

    AtriCure Recalls AtriClip LAA Exclusion System Due to Jaw Breakage

    AtriCure is recalling 464 AtriClip LAA Exclusion System devices because a complaint was received regarding the PRO2 jaw breaking prior to surgery.

    Product
    AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a conventional thermoformed polyethylene terephthalate glycol (PETG) tray with a Tyvek¿ lid. A single-walled non-corrugated box completes the single unit package. Six (6)…
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Food)·F-1450-2017·2017-02-15

    Circle U Foods Recalls Deli Sauce Seasoning Due to Glass Inclusion

    Circle U Foods is recalling 12 cases of Elmer's Deli Sauce Seasoning due to a potential glass inclusion. The product was distributed in Texas, Illinois, Kansas, and North Carolina.

    Product
    Circle U Foods, Inc. Product Code: 211013 NPP/Elmer's Deli Sauce Seasoning Pounds Per Bag/Box: 25.00 Lbs.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1177-2017·2017-02-15

    Teleflex Recalls Sheridan Cuffed Tracheal Tubes Due to Labeling Inconsistency

    Teleflex Medical is recalling Sheridan cuffed tracheal tubes because some units are labeled with incorrect sizes, potentially leading to improper airway management.

    Product
    Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A tracheal tube is inserted into a patients mouth or nose for airway management
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Food)·F-1440-2017·2017-02-15

    Dannon Dairy Drink Recalled for Incorrect Walnut Allergen Labeling

    Dannon is recalling specific bottles of Dairy Drink Nut and Cereal because the label incorrectly lists walnut as an ingredient and allergen, while the product actually contains pecan.

    Product
    DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles, UPC 36632 01421
    Category
    Food
    Distribution
    18 states