{
  "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": "Branchburg",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63312",
      "recalling_firm": "Roche Molecular Systems, Inc.",
      "address_1": "1080 Us Highway 202 S",
      "address_2": "N/A",
      "postal_code": "08876-3733",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-0489-2013",
      "product_description": "The COBAS 8000 data manager modular analyzer series (all versions)  is a is a fully automated, random-access, software- controlled system for immunoassay and photometric  analysis intended for qualitative and quantitative in-vitro determinations using a wide variety of tests.",
      "product_quantity": "77 units",
      "reason_for_recall": "Roche Molecular Systems, Inc. has become aware of a device-associated diagnostic software issue.",
      "recall_initiation_date": "20120716",
      "center_classification_date": "20121207",
      "termination_date": "20150722",
      "report_date": "20121219",
      "code_info": "Device-associated diagnostic software"
    }
  ]
}