{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "10165 McKellar Ct",
      "reason_for_recall": "The calibration for the affected batch of analyzers was incorrectly set during the manufacturing process which may lead to a failure when calibration is first performed. There may also be e remote possibility that incorrect qualitative test results for patient samples near the assay cutoff may be reported.",
      "address_2": "",
      "product_quantity": "482 units",
      "code_info": "Serial Numbers: 29003956,  29004025,  29004086,  29004072,  29004188,  29004150,  29004229,  29004127,  29004232,  29004204,  29004256,  29004362,  29004155,  29004290,  29004329,  29004347,  29004350,  29004353,  29004370,  29004390,  29004396,  29004415,  29003381,  29003814,  29004183,  29004259,  29004263,  29004281,  29004317,  29004343,  29004205,  29004209,  29004001,  29004062,  29004077,  29003915,  29004036,  29004057,  29003979,  29004085,  29004144,  29004267,  29004322,  29003960,  29003991,  29004163,  29004190,  29004330,  29003992,  29004033,  29003987,  29004306,  29004325,  29004332,  29004066,  29004335,  29004373,  29004430,  29004223,  29004299,  29003999,  29004026,  29004069,  29003811,  29004164,  29004189,  29004226,  29003923,  29004160,  29004206,  29004181,  29004194,  29003584,  29004172,  29004014,  29004046,  29004352,  29004354,  29004376,  29004285,  29004377,  29004016,  29004047,  29004054,  29004196,  29003970,  29004173,  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      "center_classification_date": "20180326",
      "distribution_pattern": "US Distribution",
      "state": "CA",
      "product_description": "Sofia 2 Analyzer Catalog Number 20299      Sofia 2 is a bench top analyzer intended to be used with Cassette-based immunofluorescent in vitro diagnostic assays . Sofia 2 is intended for professional and laboratory use.",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Quidel Corporation",
      "recall_number": "Z-1183-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79271",
      "termination_date": "20191021",
      "more_code_info": "",
      "recall_initiation_date": "20171215",
      "postal_code": "92121-4201",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}