The Recall Desk

State

New Jersey product recalls

19,788 recalls have nationwide distribution and so reach New Jersey. 0 additional recalls listed New Jersey specifically in their distribution scope.

About recalls in New Jersey

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 New Jersey 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.

2551–2575 of 19788

  • 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-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
  • HighFDA (Devices)·Z-0771-2026·2025-12-10

    [pending] Cholesterol Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0771-2026.

    Product
    Cholesterol Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0209-2026·2025-12-10

    [pending] NIVAGEN ZINC OXIDE (ZINC OXIDE)

    Pending LLM rewrite. Source: FDA_DRUG D-0209-2026.

    Product
    NIVAGEN ZINC OXIDE — NIVAGEN ZINC OXIDE (ZINC OXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0198-2026·2025-12-10

    [pending] TESTOSTERONE (TESTOSTERONE)

    Pending LLM rewrite. Source: FDA_DRUG D-0198-2026.

    Product
    TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0807-2026·2025-12-10

    [pending] Food Intolerance Test Medium

    Pending LLM rewrite. Source: FDA_DEVICE Z-0807-2026.

    Product
    Food Intolerance Test Medium
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0874-2026·2025-12-10

    [pending] Olympus OER-Mini

    Pending LLM rewrite. Source: FDA_DEVICE Z-0874-2026.

    Product
    Olympus OER-Mini
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0853-2026·2025-12-10

    [pending] IntelliVue MP40. Product Number: M8003A.

    Pending LLM rewrite. Source: FDA_DEVICE Z-0853-2026.

    Product
    IntelliVue MP40. Product Number: M8003A.
    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
  • HighFDA (Devices)·Z-0745-2026·2025-12-10

    [pending] MPOX Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0745-2026.

    Product
    MPOX 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-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-0856-2026·2025-12-10

    [pending] IntelliVue MP70. Product Number: M8007A.

    Pending LLM rewrite. Source: FDA_DEVICE Z-0856-2026.

    Product
    IntelliVue MP70. Product Number: M8007A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V793000·2025-12-10

    [pending] 2020 CHRYSLER PACIFICA

    Pending LLM rewrite. Source: NHTSA 24V793000.

    Product
    CHRYSLER — 2020 CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0761-2026·2025-12-10

    [pending] Food Sensitivity Test Medium

    Pending LLM rewrite. Source: FDA_DEVICE Z-0761-2026.

    Product
    Food Sensitivity Test Medium
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0782-2026·2025-12-10

    [pending] Gut Microbiome Test XL

    Pending LLM rewrite. Source: FDA_DEVICE Z-0782-2026.

    Product
    Gut Microbiome Test XL
    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-0858-2026·2025-12-10

    [pending] IntelliVue MP90. Product Number: M8010A.

    Pending LLM rewrite. Source: FDA_DEVICE Z-0858-2026.

    Product
    IntelliVue MP90. Product Number: M8010A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0773-2026·2025-12-10

    [pending] Akkermansia Test

    Pending LLM rewrite. Source: FDA_DEVICE Z-0773-2026.

    Product
    Akkermansia 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-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