{
  "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": "2026-07-01",
    "results": {
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    {
      "status": "Terminated",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88675",
      "recalling_firm": "Smiths Medical ASD Inc.",
      "address_1": "6000 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "UK",
      "recall_number": "Z-0163-2022",
      "product_description": "Pneupac paraPac plus 300 ventilator kit, REF P300NGB",
      "product_quantity": "2 units",
      "reason_for_recall": "Two devices were labeled with the same serial number",
      "recall_initiation_date": "20210715",
      "center_classification_date": "20211022",
      "termination_date": "20230811",
      "report_date": "20211103",
      "code_info": "SN RF70121"
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}