{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Waltham",
      "address_1": "920 Winter St",
      "reason_for_recall": "Bicarbonate Jug Adapter distributed  prior to  510(k) approval",
      "address_2": "",
      "product_quantity": "703 units",
      "code_info": "",
      "center_classification_date": "20140203",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "MA",
      "product_description": "Fresenius Bicarbonate Jug Adapter to the 2008 Series Hemodialysis machine  Part Number: 650103.    The adapter is a socket that accepts the 2008 machine spike to draw concentrate from the container.",
      "report_date": "20140212",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Fresenius Medical Care Holdings, Inc.",
      "recall_number": "Z-0920-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66953",
      "termination_date": "20210518",
      "more_code_info": "",
      "recall_initiation_date": "20131217",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}