{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Durham",
      "address_1": "100 Rodolphe St",
      "reason_for_recall": "Two batches of VIDAS Varicella-Zoster IgG (VZG ref 30217) may yield an invalid calibration which may delay the patient's sample result or a valid calibration may lead to a false positive patient result.",
      "address_2": "",
      "product_quantity": "1,218 US units total (726 US, 492 OUS)",
      "code_info": "US Model 30217-01 Lot 1007410330 and 1007393380",
      "center_classification_date": "20200207",
      "distribution_pattern": "Distributed nationwide and 9 units to Biomerieux Canada.",
      "state": "NC",
      "product_description": "VIDAS Varicella Zoster IgG (VZG) antibody IVD, kit",
      "report_date": "20200219",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "bioMerieux, Inc.",
      "recall_number": "Z-1107-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84439",
      "termination_date": "20210216",
      "more_code_info": "",
      "recall_initiation_date": "20191210",
      "postal_code": "27712-9402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}