{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98625",
      "recalling_firm": "Foundation Medicine, Inc.",
      "address_1": "150 2nd St",
      "address_2": "N/A",
      "postal_code": "02141-2115",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of Massachusetts and North Carolina.",
      "recall_number": "Z-1927-2026",
      "product_description": "Sequencing Agent SEQ0067, component of FoundationOne CDx (F1CDx)",
      "product_quantity": "163 units",
      "reason_for_recall": "Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants",
      "recall_initiation_date": "20260320",
      "center_classification_date": "20260422",
      "report_date": "20260429",
      "code_info": "Model Number: SEQ0067. Lot Numbers: 24346, 24386, 24488.",
      "more_code_info": ""
    }
  ]
}