{
  "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": "Orlando",
      "state": "FL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65070",
      "recalling_firm": "Nephron Pharmaceuticals Corp.",
      "address_1": "4121 SW 34th St",
      "address_2": "N/A",
      "postal_code": "32811-6475",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including DC and Puerto Rico and the states of AL, AZ, CA, CO, CT, FL, IL, IN, IO, GA, KS, KY, LA, MD, MN, MS, MO, NK, NV, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN , TX, VT, VA, WA, and WV, and  the countries of Guatemala, Poland, Panama, and United Kingdom.",
      "recall_number": "Z-1373-2013",
      "product_description": "EZ Breathe Medication Cup.    For the delivery of liquid medications for respiratory usage.",
      "product_quantity": "750 Medications Cups",
      "reason_for_recall": "Possible dislodgement of the \"Plate A\", if this instance occurs, it presents a potential choking hazard.",
      "recall_initiation_date": "20130430",
      "center_classification_date": "20130529",
      "termination_date": "20160628",
      "report_date": "20130605",
      "code_info": "Lots #120902, Lot # 120903 and Lot # 120904"
    }
  ]
}