{
  "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": [
    {
      "country": "United States",
      "city": "Carlsbad",
      "address_1": "2365 Camino Vida Roble",
      "reason_for_recall": "The Inspiratory valve cap on the nebulizer reservoir tower may be loose and may detach before or during treatment.",
      "address_2": "",
      "product_quantity": "8,975",
      "code_info": "Lot Numbers 042015 through 070615A  Series 8660, 8960, 8961, 8966, 8984.  Nebulizers (part numbers 8660-7, 8960-7, 8960TG-7, 8967-7, 8982-7, 8984-7), Inspiratory valve cap (part  number 600116).",
      "center_classification_date": "20150917",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and in the countries of  Greece, UK, Belgium, Australia, and Switerzland.",
      "state": "CA",
      "product_description": "NebuTech Nebulizer, Model number: Series 8660, 8960, 8961, 8966, 8984. Nebulizer used to generate aerosols delivered directly to the patient for breathing.  Designed to be used in either a hospital or homecare environment.",
      "report_date": "20150923",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Salter Labs",
      "recall_number": "Z-2781-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71909",
      "termination_date": "20160506",
      "more_code_info": "",
      "recall_initiation_date": "20150804",
      "postal_code": "92011-1505",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}