{
  "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": "70783",
      "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": "Nationwide Distribution including FL, IL, NV, NJ, OH, and TN.",
      "recall_number": "Z-2082-2015",
      "product_description": "Autopen Classic Automatic insulin delivery pen, 3.0ml x 2 unit 2-42 units, AN3800, Lot 7JH, NDC 08470-3800-01,    The product is a non-sterile automatic subcutaneous injection device which delivers insulin.",
      "product_quantity": "225 units",
      "reason_for_recall": "The dials in the Autopens are not working - the dial does not stay dialed, but springs right back to 0.  As a result, the patient could not dial up a dose of medicine to deliver via an injection.",
      "recall_initiation_date": "20141211",
      "center_classification_date": "20150715",
      "termination_date": "20170711",
      "report_date": "20150722",
      "code_info": "Lot 7JH, UPC Code 384703800014",
      "more_code_info": ""
    }
  ]
}