{
  "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": "Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72535",
      "recalling_firm": "Insulet Corporation",
      "address_1": "600 Technology Park Dr Ste 200",
      "address_2": "N/A",
      "postal_code": "01821-4126",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and countries of Switzerland, Germany, and Israel.",
      "recall_number": "Z-0394-2016",
      "product_description": "OmniPod¿, Insulin Management System (OUS)  Catalog Number: 14810     Product Usage:  The OmnniPod¿ Insulin Management System is intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin and for the quantitative measurement of glucose in fresh whole capillary blood (in vitro) from the finger.",
      "product_quantity": "5,179.0 boxes",
      "reason_for_recall": "Pod's needle mechanism fails to deploy or there is a delay in the deployment of the needle mechanism.",
      "recall_initiation_date": "20151102",
      "center_classification_date": "20151215",
      "termination_date": "20170307",
      "report_date": "20151223",
      "code_info": "Lot Codes:  L41908, L41910, F41935"
    }
  ]
}