{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Jose",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74070",
      "recalling_firm": "Stryker Corporation",
      "address_1": "5900 Optical Ct",
      "address_2": "N/A",
      "postal_code": "95138-1400",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "GA, UT, MD, NJ, MT",
      "recall_number": "Z-1910-2016",
      "product_description": "Stryker FlowPort II Adapter: Model number: 00CAT00778   The FlowPort II Adapter is intended to connect the FlowPort II Cannulas to commercially available, 4mm arthroscopes in surgical procedures.",
      "product_quantity": "21 units",
      "reason_for_recall": "Complaints were received for the Stryker FlowPort II Adapter, and investigation found that the scope sat in the adapter 180 degrees in the wrong direction",
      "recall_initiation_date": "20160504",
      "center_classification_date": "20160603",
      "termination_date": "20160603",
      "report_date": "20160615",
      "code_info": "Lot Numbers Affected: 13604"
    }
  ]
}