The Recall Desk

State

District of Columbia product recalls

19,789 recalls have nationwide distribution and so reach DC. 0 additional recalls listed District of Columbia specifically in their distribution scope.

About recalls in District of Columbia

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 District of Columbia 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 (Devices)·Z-2489-2025·2025-09-10

    [pending] RayStation with the following product descriptions: 1. RayStation 9B, Software Version: 9.1.0.93

    Pending LLM rewrite. Source: FDA_DEVICE Z-2489-2025.

    Product
    RayStation with the following product descriptions: 1. RayStation 9B, Software Version: 9.1.0.933. 2. RayStation 9B Service Pack 1, Software Version: 9.2.0.483. 3. RayStation 10A, Software Version: 10.0.0.1154. 4. RayStation 10A Service Pack 1, Software Version: 10.0
    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
  • 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-2498-2025·2025-09-10

    [pending] LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 3203

    Pending LLM rewrite. Source: FDA_DEVICE Z-2498-2025.

    Product
    LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320371500229 / 99425-000025 / 885074698953 331706400001 / 99425-000025 / 885074698953 LIFEPAK 1000: The defibrillator is to be used in AED mode only on patients who are in cardio
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0628-2025·2025-09-10

    [pending] SODIUM CHLORIDE (SODIUM CHLORIDE)

    Pending LLM rewrite. Source: FDA_DRUG D-0628-2025.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2518-2025·2025-09-10

    [pending] Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Produc

    Pending LLM rewrite. Source: FDA_DEVICE Z-2518-2025.

    Product
    Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The Merge Hemo, Model RCSV2 device is a hemodynamics recording computer system that monitors, measures, displays, records and stores various physiologic and blood fl
    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-2493-2025·2025-09-10

    [pending] RayStation with the following product descriptions: 1. RayStation 12A, Software Version: 13.0.0.

    Pending LLM rewrite. Source: FDA_DEVICE Z-2493-2025.

    Product
    RayStation with the following product descriptions: 1. RayStation 12A, Software Version: 13.0.0.1547. 2. RayStation 12A Service Pack 1, Software Version: 13.1.0.144. 3. RayStation 12A Service Pack 2, Software Version: 13.1.1.89. Product Description: Radiation Thera
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2512-2025·2025-09-10

    [pending] Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Model/Catalog Number: 9370613, 937404 Produ

    Pending LLM rewrite. Source: FDA_DEVICE Z-2512-2025.

    Product
    Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Model/Catalog Number: 9370613, 937404 Product Description: Infused with natural medical-grade honey Manuka (Leptospermum) honey is a medical-grade honey that is harvested from bees in New Zealand. Researchers have found
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2499-2025·2025-09-10

    [pending] LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 99512-001434 883873785911 LIFEPA

    Pending LLM rewrite. Source: FDA_DEVICE Z-2499-2025.

    Product
    LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 99512-001434 883873785911 LIFEPAK CR2: The LIFEPAK CR2 defibrillator is indicated for use on patients 1 year of age or older in cardiopulmonary arrest. The patient must be unresponsive (unconscious), not breathin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2448-2025·2025-09-10

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

    Pending LLM rewrite. Source: FDA_DEVICE Z-2448-2025.

    Product
    Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog Number: SW13355 Software Version: versions 2.8.0 and earlier Product Description: Dexcom G7 CGM watchOS App - The watchOS app is installed along with the iOS phone
    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·25V303000·2025-09-05

    [pending] 2024 FORD BRONCO

    Pending LLM rewrite. Source: NHTSA 25V303000.

    Product
    FORD — 2024 FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V308000·2025-09-05

    [pending] 2025 FORD BRONCO

    Pending LLM rewrite. Source: NHTSA 25V308000.

    Product
    FORD — 2025 FORD BRONCO
    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·25V304000·2025-09-05

    [pending] 2025 HEARTLAND CYCLONE

    Pending LLM rewrite. Source: NHTSA 25V304000.

    Product
    HEARTLAND — 2025 HEARTLAND CYCLONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V314000·2025-09-05

    [pending] 2023 FORD EXPEDITION

    Pending LLM rewrite. Source: NHTSA 25V314000.

    Product
    FORD — 2023 FORD EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide