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.

19626–19650 of 79143

  • HighFDA (Food)·F-0123-2023·2022-11-09

    Hood Cottage Cheese with Blueberries Recalled for Plastic Contamination

    HP Hood LLC is recalling Hood Cottage Cheese with Blueberries (16 oz) because the product may contain plastic pieces. Affected products have best-by dates between October 24, 2022 and December 12, 2022.

    Product
    Hood Cottage Cheese with Blueberries, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0172-2023·2022-11-09

    BD Trucount Tubes Recalled Due to Partial Label Detachment Causing Operational Failures

    Becton Dickinson is recalling BD Trucount Tubes due to partial label detachment that can cause tubes to stick together in pouches or fail when used with automated loaders. No illnesses have been reported.

    Product
    BD Trucount Tubes (Cat. No. 663028), used for determining absolute counts of leukocytes in blood. BD Trucount Tubes are designed for use with in vitro diagnostic products such as BD Tritest reagents, and a suitably equipped flow cytometer. BD Trucount Tubes can be used with the…
    Category
    Medical Device
    Distribution
    43 states
  • HighFDA (Food)·F-0125-2023·2022-11-09

    Hood and Penn Maid Cottage Cheese Recalled for Possible Plastic Contamination

    HP Hood LLC is recalling Hood and Penn Maid cottage cheese with pineapple and cherry due to possible plastic foreign objects. Affected products have best-by dates between October 24, 2022 and December 12, 2022.

    Product
    Hood Cottage Cheese with Pineapple & Cherry, 16 oz; Penn Maid Cottage Cheese with Pineapple & Cherry, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0170-2023·2022-11-09

    Aneurysm Embolization System Detachment Controller Recalled for Manufacturing Defect

    MICROVENTION is recalling WEB Detachment Controllers due to an out-of-specification tunnel opening that may prevent proper implant detachment. This defect could delay treatment and cause vessel damage from implant manipulation.

    Product
    WEB Detachment Controller, REF: WDC-2, WDC, MV-WDC2. Component of WEB Aneurysm Embolization System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0157-2023·2022-11-09

    Bausch + Lomb Ophthalmic Surgical Kits Recalled for Sterile Packaging Defect

    Medline Industries is recalling 800 Bausch + Lomb Basic Ophthalmic surgical kits (Lot 22DBN365) for defective breather pouch seals. Opened seals in the packaging compromise the sterile conditions required for surgical procedures.

    Product
    BAUSCH + LOMB BASIC OPHTHALMIC PACK, REF LYN023BSBLB. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0124-2023·2022-11-09

    Hood Cottage Cheese Recalled for Possible Plastic Contamination

    HP Hood is recalling Hood Cottage Cheese with Cucumber & Dill (16 oz) because the product may contain plastic foreign objects. Consumers should not eat the recalled product.

    Product
    Hood Cottage Cheese with Cucumber & Dill, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0171-2023·2022-11-09

    BD Trucount Tubes for Blood Testing Recall Due to Label Detachment

    Becton, Dickinson is recalling BD Trucount Tubes due to partial label detachment that can cause tubes to stick together or create automation errors. The defect stems from an adhesive supplier change and affects 52,570 units.

    Product
    BD Trucount Tubes (Cat. No. 340334), used for determining absolute counts of leucocytes in blood. BD Trucount tubes are designed for use with in vitro diagnostic products such as BD Tritest reagents, and a suitably equipped flow cytometer. BD Trucount tubes can be used with the…
    Category
    Medical Device
    Distribution
    43 states
  • HighNHTSA·22V830000·2022-11-09

    2023 Volkswagen ID.4 electric motor coolant leak risk

    Volkswagen is recalling 2023 ID.4 vehicles due to improper electric motor sealing assembly that may allow coolant to leak into the high-voltage system, risking loss of vehicle control and unintended airbag deployment.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0122-2023·2022-11-09

    Cottage Cheese Products Recalled Due to Possible Plastic Contamination

    HP Hood LLC is recalling multiple cottage cheese brands (Hannaford, Hood, Market Basket, Weis) due to possible plastic fragments in the products. The recall affects 391,824 cases distributed across 38 states.

    Product
    Hannaford Fat Free Cottage Cheese, 16 oz and 24 oz; Hood Fat Free Cottage Cheese, 16 oz; Market Basket Fat Free Cottage Cheese, 16 oz and 24 oz; Weis Fat Free Cottage Cheese, 24 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0148-2023·2022-11-09

    Transcutaneous monitor attachment rings recalled for weak skin adhesion

    SenTec AG voluntarily recalled 17,208 units of transcutaneous CO2/O2 monitor attachment rings due to weak skin adhesion. The devices, used in noninvasive patient monitoring, were distributed nationwide.

    Product
    sentec 24 / MARe-SF Multi-Site Attachment Ring Easy, For sensitive / fragile skin. Used in continuous, noninvasive carbon dioxide and/or oxygen tension monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0130-2023·2022-11-09

    Hood Lowfat Cottage Cheese with Peaches Recalled for Plastic Foreign Objects

    HP Hood LLC recalls Hood Lowfat Cottage Cheese with Peaches due to possible plastic foreign objects. Affected products have best-by dates between October 24, 2022 and December 12, 2022.

    Product
    Hood Lowfat Cottage Cheese with Peaches
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0156-2023·2022-11-09

    Surgical Kit Sterile Pouches with Seal Openings Recalled by Medline

    Medline is recalling approximately 160 surgical kits with defective breather pouches showing seal openings, potentially compromising sterility. The recall affects facilities in eight states nationwide.

    Product
    BAUSCH + LOMB PHACO PACK, REF LYN011PHNHD. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0146-2023·2022-11-09

    Fogarty Arterial Embolectomy Catheters Recalled for Latex Deterioration

    Edwards Lifesciences is recalling 715,620 Fogarty Arterial Embolectomy Catheters due to confirmed latex deterioration in the pouch packaging. The material degradation could affect device performance during use.

    Product
    Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP 120807FP Fogarty Arterial Embolectomy Catheter with Stylet Model Number: 120403FSP 120803FSP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0169-2023·2022-11-09

    Cardiac Navigation Catheter Recalled for Cellulose Fiber Contamination

    Johnson & Johnson is recalling 91 THERMOCOOL SMARTTOUCH SF cardiac catheters nationwide due to manufacturing defects introducing cellulose fibers into the irrigation system. The contamination may prevent proper flushing, reduce cooling capability, or cause clotting complications.

    Product
    THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac electrophysiological mapping (stimulation and recording) and, in conjunction with an RF generator, for cardiac ablation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0167-2023·2022-11-09

    NICU PICC Insertion Bundle Recalled for Breather Pouch Seal Defects

    Medline Industries recalls NICU PICC insertion bundles (50 kits) due to openings in breather pouch seals that compromise sterile barrier integrity. This Class II recall affects units distributed across the United States.

    Product
    CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O, REF CVI4470. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0024-2023·2022-11-09

    Buprenorphine and Naloxone Sublingual Tablets Recalled for Foreign Substance

    Sun Pharmaceutical is recalling buprenorphine and naloxone sublingual tablets (8 mg/2 mg) due to a foreign substance. Affected lots DNC1129A and DNC1740A were distributed nationwide.

    Product
    BUPRENORPHINE AND NALOXONE — BUPRENORPHINE AND NALOXONE (BUPRENORPHINE AND NALOXONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0129-2023·2022-11-09

    Hood Lowfat Cottage Cheese recalled due to plastic foreign objects

    HP Hood LLC is recalling Hood Lowfat Cottage Cheese (16 oz and 24 oz) with best-by dates Oct 24–Dec 12, 2022, because the product may contain plastic foreign objects.

    Product
    Hood Lowfat Cottage Cheese, 16 oz and 24 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Devices)·Z-0163-2023·2022-11-09

    Medline LINQ Surgical Trays Recalled for Compromised Pouch Seals

    Medline has recalled LINQ TRAY surgical kits with breather pouch seal openings that could compromise sterility. The recall affects 40 kits distributed nationwide; no injuries have been reported.

    Product
    MEDLINE LINQ TRAY, REF DYNJ65880A. Convenience kit used in medical/surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0160-2023·2022-11-09

    Surgical Cataract Kits Recalled for Defective Breather Pouch Seals

    Medline has recalled Bausch + Lomb cataract surgical kits due to breather pouches with seal openings that could compromise sterility. Affected kits were distributed nationwide.

    Product
    BAUSCH + LOMB CATARACT TRAY, REF LYN023FACTB. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0159-2023·2022-11-09

    Surgical eye kits recalled for breached sterile pouches

    Medline Industries recalls Bausch + Lomb eye muscle surgical kits due to breached breather pouches that may compromise sterility. The affected kits (Lot 22DBN366) were distributed nationwide.

    Product
    BAUSCH + LOMB EYE MUSCLE, REF VAL036EMESB. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0161-2023·2022-11-09

    Surgical Cataract Packs with Compromised Breather Pouch Seals Recalled

    Medline recalls 708 Bausch + Lomb cataract surgical packs due to breather pouch seal defects that could compromise sterility of surgical instruments.

    Product
    BAUSCH + LOMB CATARACT PACK, REF VAL001CPMEA. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0151-2023·2022-11-09

    Boston Scientific EMBLEM S-ICD Subcutaneous Defibrillators Software Defect Causes Battery Display Error

    Boston Scientific is recalling 7 EMBLEM S-ICD Model A209 subcutaneous defibrillators due to a software defect that displays inaccurate battery capacity information. Patients may not realize when their device's battery requires replacement.

    Product
    EMBLEM S-ICD, Subcutaneous Implantable Defibrillators, Model A209, sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0164-2023·2022-11-09

    Medline Dental Pack Recall Due to Breather Pouch Seal Defect

    Medline is recalling Dental Pack surgical kits (Lot 22DBE139) because breather pouches have openings in their seals that could compromise sterility. Affected units were distributed to healthcare facilities in eight US states.

    Product
    MEDLINE DENTAL PACK, REF DYNJ66983. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide