{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Francisco",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77607",
      "recalling_firm": "Invuity, Inc.",
      "address_1": "444 De Haro St",
      "address_2": "N/A",
      "postal_code": "94107-2347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "nationwide",
      "recall_number": "Z-2778-2017",
      "product_description": "INVUITY(R) PhotonBlade(TM), REF PB1",
      "product_quantity": "1328 units",
      "reason_for_recall": "A small number of customer observations were recently received which related to possible unintended energy discharge with the potential to cause tissue damage to patients.",
      "recall_initiation_date": "20170612",
      "center_classification_date": "20170727",
      "termination_date": "20230628",
      "report_date": "20170802",
      "code_info": "All Lot Numbers"
    }
  ]
}