The Recall Desk

State

Iowa product recalls

19,713 recalls have nationwide distribution and so reach Iowa. 0 additional recalls listed Iowa specifically in their distribution scope.

About recalls in Iowa

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 Iowa 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.

2501–2525 of 19713

  • HighFDA (Devices)·Z-0879-2026·2025-12-10

    [pending] MAMMOMAT Fusion;

    Pending LLM rewrite. Source: FDA_DEVICE Z-0879-2026.

    Product
    MAMMOMAT Fusion;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0852-2026·2025-12-10

    [pending] IntelliVue MP30. Product Number: M8002A.

    Pending LLM rewrite. Source: FDA_DEVICE Z-0852-2026.

    Product
    IntelliVue MP30. Product Number: M8002A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0212-2026·2025-12-10

    [pending] ZINC OXIDE 20% (ZINC OXIDE)

    Pending LLM rewrite. Source: FDA_DRUG D-0212-2026.

    Product
    ZINC OXIDE 20% — ZINC OXIDE 20% (ZINC OXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V798000·2025-12-10

    [pending] 2023 NISSAN Z

    Pending LLM rewrite. Source: NHTSA 24V798000.

    Product
    NISSAN — 2023 NISSAN Z
    Category
    Vehicle
    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-0727-2026·2025-12-10

    [pending] Alcohol (ALC) Test Saliva

    Pending LLM rewrite. Source: FDA_DEVICE Z-0727-2026.

    Product
    Alcohol (ALC) Test Saliva
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V795000·2025-12-10

    [pending] 2025 CADILLAC XT4

    Pending LLM rewrite. Source: NHTSA 24V795000.

    Product
    CADILLAC — 2025 CADILLAC XT4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0750-2026·2025-12-10

    [pending] Sperm Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0750-2026.

    Product
    Sperm Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0772-2026·2025-12-10

    [pending] Adrenal Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0772-2026.

    Product
    Adrenal Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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-0197-2026·2025-12-10

    [pending] PHYTONADIONE (PHYTONADIONE)

    Pending LLM rewrite. Source: FDA_DRUG D-0197-2026.

    Product
    PHYTONADIONE — PHYTONADIONE (PHYTONADIONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0792-2026·2025-12-10

    [pending] Organic acids Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0792-2026.

    Product
    Organic acids 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-0766-2026·2025-12-10

    [pending] NAD Profile Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0766-2026.

    Product
    NAD Profile Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0757-2026·2025-12-10

    [pending] Sperm Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0757-2026.

    Product
    Sperm Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0736-2026·2025-12-10

    [pending] Fecal Occult Blood Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0736-2026.

    Product
    Fecal Occult Blood Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0797-2026·2025-12-10

    [pending] Sorbitol Intolerance Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0797-2026.

    Product
    Sorbitol Intolerance Test
    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-0789-2026·2025-12-10

    [pending] Neurotransmitters Basic

    Pending LLM rewrite. Source: FDA_DEVICE Z-0789-2026.

    Product
    Neurotransmitters Basic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0728-2026·2025-12-10

    [pending] Blood Type Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0728-2026.

    Product
    Blood Type Test
    Category
    Medical Device
    Distribution
    Distributed nationwide