{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "10210 Genetic Center Dr",
      "reason_for_recall": "An incorrect incubator was installed on one Panther System which potentially led to incorrect Aptima Combo 2(R) assay (AC2) results.",
      "address_2": "",
      "product_quantity": "1 unit",
      "code_info": "Serial Number 20900001124",
      "center_classification_date": "20171018",
      "distribution_pattern": "Indiana",
      "state": "CA",
      "product_description": "Panther(R) System, Catalog Number 902615, For Use with Hologic Assays, For In Vitro Diagnostic Use",
      "report_date": "20171025",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hologic, Inc",
      "recall_number": "Z-0027-2018",
      "initial_firm_notification": "Visit",
      "product_type": "Devices",
      "event_id": "78216",
      "termination_date": "20200730",
      "more_code_info": "",
      "recall_initiation_date": "20170915",
      "postal_code": "92121-4362",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}