{
  "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": "2026-03-18",
    "results": {
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      "city": "Cambridge",
      "state": "MA",
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      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96804",
      "recalling_firm": "Foundation Medicine, Inc.",
      "address_1": "150 2nd St",
      "address_2": "N/A",
      "postal_code": "02141-2115",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "US Nationwide distribution in the state of WI.",
      "recall_number": "Z-1891-2025",
      "product_description": "FoundationOne Companion Diagnostic (F1CDx)",
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      "code_info": "Report Number: ORD-XXXXX04-01; Note: The above characters have been redacted to minimize patient information disclosure."
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