{
  "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": "Endicott",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81725",
      "recalling_firm": "SANRAI INTERNATIONAL LLC",
      "address_1": "1701 North St Ste 40",
      "address_2": "N/A",
      "postal_code": "13760-5587",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International distribution in the country of South Africa.",
      "recall_number": "Z-1058-2019",
      "product_description": "Sunset Compressor Nebulizer, Model NEB100 - Product Usage: The Sunset Compressor Nebulizer is an AC-powered air nebulizer compressor system intended to provide a source of compressed air for medical purposes for use in home healthcare. It is to be used with a nebulizer kit to produce medicated aerosol particles for respiratory therapy for both children and adults.",
      "product_quantity": "150 units",
      "reason_for_recall": "The product was designed for 120V usage and is being used in South Africa with 220V.  There is a potential for the device to overheat and the mouthpiece can pop off.",
      "recall_initiation_date": "20180829",
      "center_classification_date": "20190326",
      "termination_date": "20200612",
      "report_date": "20190403",
      "code_info": "Lot number 180223"
    }
  ]
}