{
  "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": "West Chester",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83487",
      "recalling_firm": "Aniara Diagnostica LLC",
      "address_1": "7768 Service Center Dr",
      "address_2": "N/A",
      "postal_code": "45069-2442",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distribution to US states of NC, NH, NY, and OH, and Sweden.",
      "recall_number": "Z-2346-2019",
      "product_description": "ZYMUTEST HIA MonoStrip, IgG ELISA kit, Model No. RK041A, for in vitro diagnostic use.",
      "product_quantity": "51",
      "reason_for_recall": "Residual crystallization of the microplate and recurrent negative controls out of range.",
      "recall_initiation_date": "20190719",
      "center_classification_date": "20190822",
      "termination_date": "20210611",
      "report_date": "20190828",
      "code_info": "F1701084, F1900611"
    }
  ]
}