{
  "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": "Newark",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83213",
      "recalling_firm": "Pharmaceutical Innovations, Inc.",
      "address_1": "897 Frelinghuysen Ave",
      "address_2": "N/A",
      "postal_code": "07114-2122",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US nationwide distribution including the states of AZ, CA, CT, FL,  IL,  MA, MI, MN, NC, NJ, NY, OH, PA, RI, TX, TN, VT, WV.    Distributed Internationally to accounts in Australia, France, Germany, Hong Kong, Saudi Arabia and Canada.",
      "recall_number": "Z-1970-2019",
      "product_description": "ElectroMist product codes: 36-3310-60 - Product Usage: Electrode Conductivity Spray Solution.",
      "product_quantity": "8982",
      "reason_for_recall": "Potential for failed stability antimicrobial effectiveness testing.",
      "recall_initiation_date": "20190619",
      "center_classification_date": "20190712",
      "termination_date": "20200729",
      "report_date": "20190724",
      "code_info": "Lot # 051914-60, 101615-60, 021317-60"
    }
  ]
}