The Recall Desk

State

New Hampshire product recalls

19,789 recalls have nationwide distribution and so reach New Hampshire. 0 additional recalls listed New Hampshire specifically in their distribution scope.

About recalls in New Hampshire

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 Hampshire 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.

3726–3750 of 19789

  • HighFDA (Drugs)·D-0614-2025·2025-09-10

    [pending] KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion After Dilution, Sing

    Pending LLM rewrite. Source: FDA_DRUG D-0614-2025.

    Product
    KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion After Dilution, Single-Does vial. Mfd by: Immunocore Limited, 92 Park Drive, Abingdon, Oxfordshire, OX14 4RY, United Kingdom, For: Immunocore Commercial LLC, 181 Washington St, Conshohocken, PA, 19428
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2521-2025·2025-09-10

    [pending] MI Cancer Seek REF MSC000 UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Seek is a single-s

    Pending LLM rewrite. Source: FDA_DEVICE Z-2521-2025.

    Product
    MI Cancer Seek REF MSC000 UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Seek is a single-site assay intended to provide tumor mutational profiling to be used by qualified healthcare professionals in accordance with professional oncology guidelines for cancer patients wi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2515-2025·2025-09-10

    [pending] Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Platelia Toxo IgM assay is a

    Pending LLM rewrite. Source: FDA_DEVICE Z-2515-2025.

    Product
    Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Platelia Toxo IgM assay is a semi-quantitative immunocapture enzyme immunoassay kit for the detection of IgM antibodies to Toxoplasma gondii in human serum, plasma or cord blood specimens.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2517-2025·2025-09-10

    [pending] FloPatch FP120, REF: FP120-FOT01-005

    Pending LLM rewrite. Source: FDA_DEVICE Z-2517-2025.

    Product
    FloPatch FP120, REF: FP120-FOT01-005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2506-2025·2025-09-10

    [pending] Brand Name: MediHoney ¿ Product Name: MediHoney ¿ Tube Model/Catalog Number: 31515 and 31535 Prod

    Pending LLM rewrite. Source: FDA_DEVICE Z-2506-2025.

    Product
    Brand Name: MediHoney ¿ Product Name: MediHoney ¿ Tube Model/Catalog Number: 31515 and 31535 Product Description: MediHoney¿ Paste with Active Leptospermum Honey is a moist dressing made of 100% Active Leptospermum medical grade Honey. The dressing helps maintain a moist envir
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2492-2025·2025-09-10

    [pending] RayStation with the following product descriptions: 1. RayStation 11B, Software Version: 12.0.0.

    Pending LLM rewrite. Source: FDA_DEVICE Z-2492-2025.

    Product
    RayStation with the following product descriptions: 1. RayStation 11B, Software Version: 12.0.0.932. 2. RayStation 11B Service Pack 1, Software Version: 12.1.0.1221. 3. RayStation 11B Service Pack 2, Software Version: 12.0.3.68. 4. RayStation 11B Service Pack 3, Soft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2497-2025·2025-09-10

    [pending] LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2

    Pending LLM rewrite. Source: FDA_DEVICE Z-2497-2025.

    Product
    LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022 V15-2-000099 / 99577-000093 / 883873979020 V15-2-001603 / 99577-001256 / 883873911631 LIFEPAK 15: The LP15 is intended for use by trained
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2494-2025·2025-09-10

    [pending] RayStation with the following product descriptions: 1. RayStation 6 Service Pack 1, Software Ver

    Pending LLM rewrite. Source: FDA_DEVICE Z-2494-2025.

    Product
    RayStation with the following product descriptions: 1. RayStation 6 Service Pack 1, Software Version: 6.1.1.2. 2. RayStation 6 Service Pack 2, Software Version: 6.2.0.7. 3. RayStation 6 Service Pack 3, Software Version: 6.3.0.6. Product Description: Radiation Thera
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V786000·2025-09-10

    [pending] 2025 BRINKLEY RV MODEL G

    Pending LLM rewrite. Source: NHTSA 24V786000.

    Product
    BRINKLEY RV — 2025 BRINKLEY RV MODEL G
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2485-2025·2025-09-10

    [pending] Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529

    Pending LLM rewrite. Source: FDA_DEVICE Z-2485-2025.

    Product
    Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect Decompression System 10MM, VF Implant 101-9810 00884662000536 Superion Indirect Decompression System 12MM, VF Implant 101-9812 00884662000543 Superion
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2495-2025·2025-09-10

    [pending] RayStation with the following product descriptions: 1. RayStation 2023B, Software Version: 14.0.

    Pending LLM rewrite. Source: FDA_DEVICE Z-2495-2025.

    Product
    RayStation with the following product descriptions: 1. RayStation 2023B, Software Version: 14.0.0.3338. 2. RayStation 2024A, Software Version: 15.0.0.430. 3. RayStation 2024A SP3, Software Version: 15.1.3.10. Product Description: Radiation Therapy Treatment Plannin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2446-2025·2025-09-10

    [pending] Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM Android App

    Pending LLM rewrite. Source: FDA_DEVICE Z-2446-2025.

    Product
    Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM Android App Model/Catalog Number: SW12299 Software Version: version 2.8.0 and earlier Product Description: Dexcom G7 CGM Android App SW12299 Component: Dexcom G7 Continuous Glucose Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2449-2025·2025-09-10

    [pending] Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ Android CGM

    Pending LLM rewrite. Source: FDA_DEVICE Z-2449-2025.

    Product
    Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ Android CGM App Model/Catalog Number: SW14245 Software Version: versions 1.4.0 and earlier Product Description: Dexcom ONE+ Androind CGM App Component: Dexcom ONE+ Continuous Glucose Monit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V626000·2025-09-08

    [pending] 2024 CHEVROLET SILVERADO 1500

    Pending LLM rewrite. Source: NHTSA 24V626000.

    Product
    CHEVROLET — 2024 CHEVROLET SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V624000·2025-09-08

    [pending] 2024 ESCAPE ESCAPE 5.0

    Pending LLM rewrite. Source: NHTSA 24V624000.

    Product
    ESCAPE — 2024 ESCAPE ESCAPE 5.0
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V312000·2025-09-05

    [pending] 2021 FORD BRONCO

    Pending LLM rewrite. Source: NHTSA 25V312000.

    Product
    FORD — 2021 FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V315000·2025-09-05

    [pending] 2023 LINCOLN CORSAIR

    Pending LLM rewrite. Source: NHTSA 25V315000.

    Product
    LINCOLN — 2023 LINCOLN CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V310000·2025-09-05

    [pending] 2025 FORD RANGER

    Pending LLM rewrite. Source: NHTSA 25V310000.

    Product
    FORD — 2025 FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V316000·2025-09-05

    [pending] 2025 LINCOLN AVIATOR

    Pending LLM rewrite. Source: NHTSA 25V316000.

    Product
    LINCOLN — 2025 LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V306000·2025-09-05

    [pending] 2025 FORD F-250 SD

    Pending LLM rewrite. Source: NHTSA 25V306000.

    Product
    FORD — 2025 FORD F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide