{
  "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": "Chelmsford",
      "address_1": "269 Mill Road",
      "reason_for_recall": "Shipped with incorrect software",
      "address_2": "",
      "product_quantity": "11 units",
      "code_info": "Serial Numbers:  AR11J000164,  AR12E000853,  AR12E000856, AR12E000868,  AR12E000920,  AR12E000922,  AR12E000923,  AR12E000931, AR12E000944   AR12F001100,  AR12F001298,",
      "center_classification_date": "20120917",
      "distribution_pattern": "Worldwide Distribution - US Nationwide including the states of: LA, MA, ME, NC, ND, NE, OH and the country of Germany.",
      "state": "MA",
      "product_description": "Zoll X Series Defibrillator/Pacemaker/Monitor    Product Usage:  The product is used by qualified medical personnel for the purpose of converting ventricular fibrillation to sinus rhythm or other cardiac rhythms capable of producing hemodynamically significant heart beats. In addition, the product may be used in synchronized mode to terminate certain atrial and ventricular tachycardias and other arrhythmias resistant to drug therapy. The X Series may be used for cardiac pacing in conscious or unconscious patients for up to a few hours duration as an alternative to endocardial stimulation. The X Series may be used for the monitoring a patient\u0019s electrocardiogram (ECG).",
      "report_date": "20120926",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ZOLL Medical Corporation",
      "recall_number": "Z-2401-2012",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "63004",
      "termination_date": "20120919",
      "more_code_info": "",
      "recall_initiation_date": "20120816",
      "postal_code": "01824",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}