The Recall Desk

State

Kansas product recalls

73,388 recalls have nationwide distribution and so reach Kansas. 5,755 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,755
Critical
1,056
Severe
1,477
Most recent
2026-09-30

Of the 5,755 recalls naming Kansas we have scored against our rubric, 1,056 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,477 (26%) are Severe.

These figures cover only the 5,755 recalls whose distribution notice names Kansas specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19651–19675 of 79143

  • HighFDA (Devices)·Z-0155-2023·2022-11-09

    Surgical Eye Kit Pouches Recalled for Seal Defects

    Medline recalls Bausch + Lomb Eye surgical kits due to breather pouches with openings in the seal. Affected kits were distributed to healthcare facilities nationwide; unopened kits should not be used.

    Product
    BAUSCH + LOMB EYE PACK, REF LYN003EYSPA. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0166-2023·2022-11-09

    Medline CVC Barrier Kit Recalled for Breached Pouch Seals

    Medline is recalling CVC barrier kits (Lot 22ABT774) due to breather pouches with seal openings that could compromise sterility of the surgical kit contents.

    Product
    MEDLINE CVC BARRIER KIT, REF DYNJ80485. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0131-2023·2022-11-09

    Lactaid Cottage Cheese Recalled for Plastic Foreign Objects

    HP Hood LLC is recalling Lactaid Cottage Cheese (16 oz) with best-by dates Oct 24 2022 to Dec 12 2022 due to possible plastic contamination. Consumers should discard or return affected products.

    Product
    Lactaid Cottage Cheese, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0165-2023·2022-11-09

    Medline Radiology Procedure Pack Breather Pouches Recalled for Seal Defects

    Medline is recalling 240 Radiology Procedure Packs because some breather pouches show seal openings that could compromise sterility. The affected kits were distributed nationwide.

    Product
    MEDLINE RADIOLOGY PROCEDURE PACK, REF DYNJ67150A. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0128-2023·2022-11-09

    Hood Cottage Cheese with Pineapple Recalled for Possible Plastic Contamination

    HP Hood LLC is recalling Hood Fat Free Cottage Cheese with Pineapple, 16 oz containers for possible plastic contamination. Affected products have best-by dates from October 24, 2022 through December 12, 2022.

    Product
    Hood Fat Free Cottage Cheese with Pineapple, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Food)·F-0127-2023·2022-11-09

    Hood Everything Bagel Cottage Cheese Recalled for Plastic Fragments

    HP Hood LLC is recalling Hood Everything Bagel Cottage Cheese due to the potential presence of plastic fragments. The recall affects approximately 391,824 cases distributed across 37 states with best-by dates from October 24 to December 12, 2022.

    Product
    Hood Everything Bagel Cottage Cheese, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0152-2023·2022-11-09

    Implantable Defibrillator Software Error Causes Inaccurate Battery Display

    Boston Scientific's EMBLEM MRI S-ICD implantable defibrillators contain a software defect with an incorrect manufacturing date that causes inaccurate battery capacity display. The recall affects 142 devices distributed worldwide.

    Product
    EMBLEM MRI S-ICD, Subcutaneous Implantable Defibrillator, Model A219, sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0121-2023·2022-11-09

    Cottage Cheese with Pineapple Recalled for Plastic Contamination

    HP Hood LLC is recalling multiple brands of cottage cheese with pineapple due to possible plastic contamination. Products with best-by dates between October 24 and December 12, 2022 were distributed across 38 states.

    Product
    Food Club Cottage Cheese with Pineapple, 16 oz; Hannaford Cottage Cheese with Pineapple, 16 oz; Hood Cottage Cheese with Pineapple, 16 oz and 24 oz; Market Basket Cottage Cheese with Pineapple, 16 oz; Penn Maid Cottage Cheese with Pineapple, 16 oz;
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0162-2023·2022-11-09

    Medline Lithotomy Sterile Surgical Kit Recalled for Compromised Breather Pouch Seal

    Medline is recalling 96 sterile surgical kits (REF DYNJ50099C, Lot 22DBL482) distributed nationwide due to complaints of openings in breather pouches that compromise sterility and increase contamination risk.

    Product
    MEDLINE LITHOTOMY, REF DYNJ50099C. Convenience kit used in medical/surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0119-2023·2022-11-09

    HP Hood Chive Cottage Cheese Recalled for Plastic Contamination

    HP Hood LLC is recalling chive cottage cheese sold under multiple store brands due to potential plastic contamination. Approximately 391,824 cases distributed across 37 states.

    Product
    Food Club Chive Cottage Cheese, 16 oz; Hannaford Chive Cottage Cheese, 16 oz; Hood Chive Cottage Cheese, 16 oz and 24 oz; Price Chopper Chive Cottage Cheese, 16 oz; Market Basket CChive Cottage Cheese, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0147-2023·2022-11-09

    Fogarty Biliary Balloon Probes recalled for latex deterioration

    Edwards Lifesciences is recalling Fogarty Biliary Balloon Probes due to confirmed latex deterioration in pouches. The recall affects 26,560 units distributed worldwide.

    Product
    Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0168-2023·2022-11-09

    Pediatric Vision Scanner Battery Pack Poses Fire Risk

    Rebiscan is recalling Blinq Pediatric Vision Scanners (Model BQ830) because the battery pack may vent and catch fire if a cell voltage drops below 2.5V.

    Product
    Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for automated detection of misalignment of the visual axes using polarized light. Model Number BQ830
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0025-2023·2022-11-09

    Ranibizumab eye implant recalled for non-functioning delivery system

    Genentech is recalling Susvimo ocular implants (452 units nationwide) due to manufacturing defects in the drug delivery system. A few patients have experienced non-functioning implants.

    Product
    SUSVIMO — SUSVIMO (RANIBIZUMAB)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0173-2023·2022-11-09

    BD Multitest 6-Color TBNK tubes recalled for partial label detachment

    BD Multitest 6-Color TBNK tubes are being recalled due to partial label detachment. The defect can cause tubes to stick together or lead to automation errors when used with the flow cytometer's automated loader.

    Product
    BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995), for use with BD FACSLyric, BD FACSCanto II, and BD FACSCanto flow cytometers to determine the percentages and absolute counts of human lymphocyte subsets in peripheral whole blood for immunophenotyping.
    Category
    Medical Device
    Distribution
    43 states
  • HighNHTSA·22V828000·2022-11-04

    Forest River Recalls 2022-2023 East to West Alta Travel Trailers

    Forest River is recalling 2022-2023 East to West Alta travel trailers because side marker lights may not reflect light as intended, reducing visibility.

    Product
    EAST TO WEST — EAST TO WEST ALTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23034·2022-11-03

    BLACK+DECKER Garment Steamers Recalled for Burn Hazard from Hot Water

    Empower Brands recalls about 518,500 BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, posing a burn hazard. The company has received 241 reports of hot water expelling, including 32 reports of burn injuries.

    Product
    BLACK+DECKER Model HGS011 Easy Garment Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23032·2022-11-03

    FUUL Lamp Oil Recalled for Non-Child-Resistant Packaging and Labeling Failures

    FHS Retail is recalling about 1,700 units of FUUL 1.9L Pure Liquid Paraffin Lamp Oil because the packaging is not child-resistant and the label omits mandatory safety information required by federal law. The product can cause fatal chemical pneumonia or lung damage if ingested.

    Product
    FUUL 1.9L Pure Liquid Paraffin Lamp Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V825000·2022-11-03

    2021-2022 Ford Bronco Rearview Camera Display May Distract Drivers

    Ford is recalling 2021-2022 Bronco vehicles with rearview camera systems because the camera image may remain displayed after the vehicle shifts out of reverse, potentially distracting drivers and increasing crash risk.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23035·2022-11-03

    AirWick Fresh New Day Aerosol Air Fresheners Recalled for Rupture and Laceration Risk

    Reckitt is recalling about 67,000 AirWick Fresh New Day aerosol air fresheners in Fresh Linen and Fresh Waters scents due to a missing corrosion inhibitor in one batch that can cause cans to rupture or leak. No injuries have been reported.

    Product
    AirWick Fresh New Day® aerosol air fresheners - "Fresh Linen" and "Fresh Waters" scents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23036·2022-11-03

    Clarks Women's Navy Canvas Shoes Recalled for Chemical Hazard

    Clarks Americas is recalling three styles of women's navy canvas shoes sold from February to October 2022 because prolonged contact with the shoe material can expose wearers to toxic chemicals benzidine and/or dimethoxybenzidine.

    Product
    Breeze Ave, Breeze Shore and Breeze Step women's shoes in navy colors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V827000·2022-11-03

    2021 Cadillac Escalade daytime running lights control software defect

    General Motors is recalling 2021 Cadillac Escalade vehicles. The daytime running lights may not deactivate when headlights are on, which may cause glare and reduce visibility, increasing crash risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SUBURBAN, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide