{
  "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": [
    {
      "country": "United States",
      "city": "Woburn",
      "address_1": "10a Roessler Rd",
      "reason_for_recall": "Kits incompatible with certain fluorescence microscope light sources",
      "address_2": "",
      "product_quantity": "49 kits US; 17 kits OUS",
      "code_info": "Lot codes US:  04813C, 7413, 08113  exp. 2013-12    Lot codes OUS:  03113A  04213A  04813B",
      "center_classification_date": "20140102",
      "distribution_pattern": "Worldwide Distribution - USA including CA, IL, IN,  OH, NJ, MI , MO, NY, WI.  Internationally to Denmark.",
      "state": "MA",
      "product_description": "AdvanDx Gram-Negative QuickFISH BC.   In-Vitro Diagnostic for the identification of Enterobacteriacae  Catalog Number: QFGNRBC1-25    Gram-Negative QuickFISH BC provides rapid identification of Escherichia coli, and/or Pseudomonas aeruginosa, and/or Klebsiella pneumoniae directly from GNR-positive blood cultures",
      "report_date": "20140108",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "AdvanDx, Inc.",
      "recall_number": "Z-0619-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67069",
      "termination_date": "20140113",
      "more_code_info": "",
      "recall_initiation_date": "20131211",
      "postal_code": "01801-6208",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}