{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Brooklyn",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80030",
      "recalling_firm": "Respire Medical",
      "address_1": "18 Bridge St Ste 4J",
      "address_2": "N/A",
      "postal_code": "11201-1107",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide distribution.",
      "recall_number": "Z-1950-2018",
      "product_description": "Respire Pink H/S Oral Sleep Apnea Device",
      "product_quantity": "N/A",
      "reason_for_recall": "Potential for device breakage during use",
      "recall_initiation_date": "20170901",
      "center_classification_date": "20180529",
      "termination_date": "20191209",
      "report_date": "20180606",
      "code_info": "Serial Number: 46299"
    }
  ]
}