{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Dover",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64464",
      "recalling_firm": "Churchill Medical Systems, Inc.",
      "address_1": "87 Venture Drive",
      "address_2": "N/A",
      "postal_code": "03820-5914",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including MO, IL, FL, PA, VA, MO, NY, NE, NH, and OH.",
      "recall_number": "Z-0914-2013",
      "product_description": "Lifeguard Infusion Set with Smartsite, 20Ga, 1, CLGY-2010    Huber type needle set used for the infusion of medical fluids into implantable ports.",
      "product_quantity": "2340",
      "reason_for_recall": "The label on the device states that the item number is CLGY-2210 when the item number on the device label should read CLGY-2010. This is a 20Ga Huber needle set; however, the product label states the pouch contains a 22Ga set.",
      "recall_initiation_date": "20130121",
      "center_classification_date": "20130306",
      "termination_date": "20130910",
      "report_date": "20130313",
      "code_info": "Lot #1210099"
    }
  ]
}