{
  "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 Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76337",
      "recalling_firm": "Quidel Corporation",
      "address_1": "10165 McKellar Ct",
      "address_2": "N/A",
      "postal_code": "92121-4201",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution to FL, GA, IL, IN, KY, MT, OH, PA, TX",
      "recall_number": "Z-1231-2017",
      "product_description": "Influenza Transport Swab Packages, Reference #20171,  One lot with 1010 packages (each package contains 25 transport tubes).    The Influenza Swabs in dry transport tubes are intended for use with influenza tests",
      "product_quantity": "1,010 packages",
      "reason_for_recall": "Quidel Corporation is recalling Influenza Transport Swab Packages because it may include an incorrect sample swab mixed in with the proper swabs.",
      "recall_initiation_date": "20170125",
      "center_classification_date": "20170222",
      "termination_date": "20170602",
      "report_date": "20170301",
      "code_info": "PS10171"
    }
  ]
}