{
  "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": [
    {
      "status": "Terminated",
      "city": "Framingham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68821",
      "recalling_firm": "Ab Sciex",
      "address_1": "500 Old Connecticut Path",
      "address_2": "N/A",
      "postal_code": "01701-4574",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "FL, NC, OK, PA, TX",
      "recall_number": "Z-2609-2014",
      "product_description": "AB SCIEX API 3200MD\" LC/MS/MS System with software:   MultiQuantMD  3.0In vitro diagnostic to identify inorganic or organic compounds (e.g., lead, mercury, and drugs) in human specimens  Part Number 5024543.",
      "product_quantity": "6 units",
      "reason_for_recall": "Software- AB SCIEX API 3200MD LC/MS/MS SYSTEM with MultiQuantMD 3.0 software may provide incorrect data for patient diagnosis",
      "recall_initiation_date": "20140715",
      "center_classification_date": "20140908",
      "termination_date": "20141001",
      "report_date": "20140917",
      "code_info": "Serial Numbers:  BV20031308, BV20081311, BV20051310, BV20071311, BV20101401,  BV20131401"
    }
  ]
}