{
  "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,
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  "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-0485-2013",
      "product_description": "The MagNA Pure LC (version 3.0) is a sample preparation  instrument  that can be used with the LightCycler instrument for automated isolation of nucleic acids in various types of biological materials.",
      "product_quantity": "816 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"
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}