{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Exeter",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69116",
      "recalling_firm": "Vapotherm, Inc.",
      "address_1": "22 Industrial Dr Ste 1",
      "address_2": "N/A",
      "postal_code": "03833-4557",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to Canada, France, Swizerland, Korea, Sweden, Germany , Belgium, Spain, Mexico, Scotland, UAE, Australia, Israel, Hong Kong, Ireland, kuwait, and Italy.",
      "recall_number": "Z-2704-2014",
      "product_description": "Vapotherm Precision Flow,Disposable Patient Circuit  PF-E-DPC-Low.  PF-DPC-Low packaged with compatible cannulas for evaluation of the  Precision Flow system",
      "product_quantity": "360 units",
      "reason_for_recall": "Disposable Patient Circuit that allows water  to leak into the center gas lumen",
      "recall_initiation_date": "20140813",
      "center_classification_date": "20140925",
      "termination_date": "20151002",
      "report_date": "20141001",
      "code_info": "Lot Numbers 1402021 through 1406010, excluding lots 1402024 through 1402028 and 1404003. These numbers are applicable regardless of the prefix preceding them (i.e. HF, HFE, HFH, HFN, LF, LFE, LFH or LFN)."
    }
  ]
}