The Recall Desk

State

Kansas product recalls

19,787 recalls have nationwide distribution and so reach Kansas. 0 additional recalls listed Kansas specifically in their distribution scope.

About recalls in Kansas

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Kansas consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

2651–2675 of 19787

  • HighFDA (Devices)·Z-0796-2026·2025-12-10

    [pending] SIBO Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0796-2026.

    Product
    SIBO Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0216-2026·2025-12-10

    [pending] DULOXETINE (DULOXETINE HYDROCHLORIDE)

    Pending LLM rewrite. Source: FDA_DRUG D-0216-2026.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0730-2026·2025-12-10

    [pending] Chlamydia Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0730-2026.

    Product
    Chlamydia Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0810-2026·2025-12-10

    [pending] Iodine Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0810-2026.

    Product
    Iodine Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0731-2026·2025-12-10

    [pending] D-Dimer Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0731-2026.

    Product
    D-Dimer Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0804-2026·2025-12-10

    [pending] Allergy test Small

    Pending LLM rewrite. Source: FDA_DEVICE Z-0804-2026.

    Product
    Allergy test Small
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0806-2026·2025-12-10

    [pending] Food Intolerance Test Large

    Pending LLM rewrite. Source: FDA_DEVICE Z-0806-2026.

    Product
    Food Intolerance Test Large
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0776-2026·2025-12-10

    [pending] DHEA Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0776-2026.

    Product
    DHEA Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0770-2026·2025-12-10

    [pending] Continuous Glucose Monitor (CGM)

    Pending LLM rewrite. Source: FDA_DEVICE Z-0770-2026.

    Product
    Continuous Glucose Monitor (CGM)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0765-2026·2025-12-10

    [pending] Mycotoxin Panel Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0765-2026.

    Product
    Mycotoxin Panel Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0734-2026·2025-12-10

    [pending] Drug Test Small (4 substances)

    Pending LLM rewrite. Source: FDA_DEVICE Z-0734-2026.

    Product
    Drug Test Small (4 substances)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0803-2026·2025-12-10

    [pending] Allergy test Small

    Pending LLM rewrite. Source: FDA_DEVICE Z-0803-2026.

    Product
    Allergy test Small
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0768-2026·2025-12-10

    [pending] Vitamin D2 and D3 Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0768-2026.

    Product
    Vitamin D2 and D3 Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0813-2026·2025-12-10

    [pending] Pet Allergy Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0813-2026.

    Product
    Pet Allergy Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0793-2026·2025-12-10

    [pending] Parasite Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0793-2026.

    Product
    Parasite Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0816-2026·2025-12-10

    [pending] 2 in 1 Trichomonas / Gardnerella Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0816-2026.

    Product
    2 in 1 Trichomonas / Gardnerella Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0738-2026·2025-12-10

    [pending] Gonorrhea test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0738-2026.

    Product
    Gonorrhea test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0769-2026·2025-12-10

    [pending] Allergy Test IgE

    Pending LLM rewrite. Source: FDA_DEVICE Z-0769-2026.

    Product
    Allergy Test IgE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0725-2026·2025-12-10

    [pending] InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure ONE POL Patient Kit - 10 pack

    Pending LLM rewrite. Source: FDA_DEVICE Z-0725-2026.

    Product
    InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure ONE POL Patient Kit - 10 pack. Model Number: 90010. 2. Insure ONE POL Patient Kit - 25 Pack. Model Number: 90025. 3. InSure ONE POL Combo Pack. Model Number: 90030. InSure ONE is a fecal immunochemica
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0755-2026·2025-12-10

    [pending] Vaginal PH Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0755-2026.

    Product
    Vaginal PH Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0814-2026·2025-12-10

    [pending] Pollen Allergy Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0814-2026.

    Product
    Pollen Allergy Test
    Category
    Medical Device
    Distribution
    Distributed nationwide