{
  "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": "Lexington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74732",
      "recalling_firm": "T2 Biosystems Inc",
      "address_1": "101 Hartwell Ave",
      "address_2": "N/A",
      "postal_code": "02421-3125",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed to the states of UT, FL, NH, PA, GA, MI, AL, IN, NJ, CA, NY, LA, RI, TN, TX, WI, and CT.",
      "recall_number": "Z-2795-2016",
      "product_description": "T2Candida¿Cartridges; Part Number: 90-01794 (box of 12) and Part Number: 91-01534 (individual cartridge base).    A qualitative T2 Magnetic Resonance (T2MR¿) assay for the direct detection of Candida species in EDTA human whole blood specimens.",
      "product_quantity": "6,864",
      "reason_for_recall": "Elevated levels of invalid results.",
      "recall_initiation_date": "20160707",
      "center_classification_date": "20160914",
      "termination_date": "20171006",
      "report_date": "20160921",
      "code_info": "Lot Numbers:   000048532541  000048730657  000049837721  000050205643  000050205642  000050205641  000050205644  000051259462  000051269868  000051807669  000051989614  000052596978",
      "more_code_info": ""
    }
  ]
}