{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Marietta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70665",
      "recalling_firm": "Owen Mumford USA, Inc.",
      "address_1": "1755 W Oak Commons Ct",
      "address_2": "N/A",
      "postal_code": "30062-2280",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide distribution in the states of AL, AR, CA, FL, GA, IL, MO, NC, OK, TN, and TX.",
      "recall_number": "Z-1366-2015",
      "product_description": "Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010    The Autoject E1 is an injector used by patients to inject drugs as prescribed by their doctor.",
      "product_quantity": "3,100",
      "reason_for_recall": "The syringe carrier is missing components: a damper and spring.",
      "recall_initiation_date": "20141124",
      "center_classification_date": "20150402",
      "termination_date": "20170731",
      "report_date": "20150408",
      "code_info": "Lot No. 5LW"
    }
  ]
}