{
  "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": [
    {
      "status": "Terminated",
      "city": "Durham",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89568",
      "recalling_firm": "bioMerieux, Inc.",
      "address_1": "100 Rodolphe St",
      "address_2": "N/A",
      "postal_code": "27712-9402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to CA, FL, GA, IL, IN, LA, MA, MD, ME, MO, NJ, NY, OH, PA, TX, VA, WI, and WV.  There was government distribution but no military or foreign distribution.",
      "recall_number": "Z-0742-2022",
      "product_description": "VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx.",
      "product_quantity": "480 kits",
      "reason_for_recall": "Invalid calibrations (out of range high) while using the product.",
      "recall_initiation_date": "20220209",
      "center_classification_date": "20220314",
      "termination_date": "20260401",
      "report_date": "20221005",
      "code_info": "Lot numbers 1008873260, exp. 01JUN2022."
    }
  ]
}