{
  "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": [
    {
      "status": "Terminated",
      "city": "Athens",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79595",
      "recalling_firm": "Diagnostic Hybrids, Inc.",
      "address_1": "2005 E State St Ste 100",
      "address_2": "N/A",
      "postal_code": "45701-2125",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The product was distributed to the following countries: Singapore, Switzerland",
      "recall_number": "Z-1520-2018",
      "product_description": "Quidel MicroVue Intact PTH EIA, Model 8044.  An enzyme immunoassay for the quantification of Intact Parathyroid Hormone (PTH) in serum.",
      "product_quantity": "26",
      "reason_for_recall": "There may be a loss of separation between Calibrators A and B which may impact the assay calibration at the lower end of the assay.",
      "recall_initiation_date": "20161026",
      "center_classification_date": "20180425",
      "termination_date": "20200828",
      "report_date": "20180502",
      "code_info": "Lot 068259"
    }
  ]
}