{
  "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": [
    {
      "country": "United States",
      "city": "Framingham",
      "address_1": "500 Old Connecticut Path",
      "reason_for_recall": "Wrong quantitative results may be displayed in a report from the device, which may potentially lead to an incorrect patient diagnosis.",
      "address_2": "",
      "product_quantity": "279",
      "code_info": "Software Versions: Version 1.6.1 and 1.6.2",
      "center_classification_date": "20160429",
      "distribution_pattern": "Worldwide Distribution - US (Nationwide) and Internationally to the following countries:  AUSTRIA  CANADA  CHINA  FRANCE  GERMANY  INDIA  IRELAND  ITALY  KOREA  MALAYSIA  NETHERLANDS  NORWAY  RUSSIA  SINGAPORE  SPAIN  SWITZERLAND  UNITED KINGDOM",
      "state": "MA",
      "product_description": "Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the following instruments: API 3200MD\" LC/MS/MS System, Instrument Part Number: 5024501; 3200MD QTRAP¿ LC/MS/MS System, Instrument Part Number:  5024500; Triple Quad\" 4500MD LC/MS/MS System, Instrument Part Number:  5031257; QTRAP¿ 4500MD LC/MS/MS System, Instrument Part Number:  5031231  3200MD series and 4500MD series are mass spectrometers intended to identify inorganic or organic compounds (e.g., lead, mercury, and drugs) in human specimens by ionizing the compound under investigation and separating the resulting ions by means of an electrical and magnetic field according to their mass. It is intended for in vitro diagnostic purposes. For in vitro diagnostic use.",
      "report_date": "20160511",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ab Sciex",
      "recall_number": "Z-1586-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73433",
      "termination_date": "20170206",
      "more_code_info": "",
      "recall_initiation_date": "20160224",
      "postal_code": "01701-4574",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}