{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Abbott Park",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71473",
      "recalling_firm": "Abbott Laboratories",
      "address_1": "100 Abbott Park Rd",
      "address_2": "N/A",
      "postal_code": "60064-3502",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide Distribution in the states of CA, AL, NY and WI.",
      "recall_number": "Z-2202-2015",
      "product_description": "ARCHITECT c8000 System List Number 01G06-98    Product Usage:  The Abbott ARCHITECT cSystem is intended for In Vitro diagnostic use only. It is designed to perform automated: chemistry tests, utilizing photometry and potentiometric technology.",
      "product_quantity": "5 units",
      "reason_for_recall": "The ARCHITECT c8000 instrument contains tubing that does not meet specifications and has the potential to leak.",
      "recall_initiation_date": "20150611",
      "center_classification_date": "20150722",
      "termination_date": "20160209",
      "report_date": "20150729",
      "code_info": "Serial Numbers: C802239, C802312, C802260, C802447, C801911"
    }
  ]
}