{
  "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": "Chelmsford",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67749",
      "recalling_firm": "ZOLL Medical Corporation",
      "address_1": "269 Mill Road",
      "address_2": "N/A",
      "postal_code": "01824",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to Canada, AE, Afganistian, Australia, Belgium, Czech Republic , China, Chile, Croatia, Denmark, France, Great Britain, Hungary, Israel, Italy, Japan, Korea, Kuwait, Russia, Saudi Arabia, Singapore, South Africa,Thailand, and Turkey.",
      "recall_number": "Z-1311-2014",
      "product_description": "Zoll Medical X Series, PropaqMD, PropaqM   Defibrillator/Pacemaker/Monitor  With System Software Version 02.10.02.00 or Higher, automated external defibrillator.",
      "product_quantity": "3,169 units",
      "reason_for_recall": "Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop and cannot be used",
      "recall_initiation_date": "20140305",
      "center_classification_date": "20140331",
      "termination_date": "20210129",
      "report_date": "20140409",
      "code_info": "System Software Version 02.10.02.00 or Higher"
    }
  ]
}