{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Pittsburgh",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78926",
      "recalling_firm": "Zoll Manufacturing Corp.",
      "address_1": "121 Gamma Dr",
      "address_2": "N/A",
      "postal_code": "15238-2919",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide",
      "recall_number": "Z-0353-2018",
      "product_description": "LifeVest Wearable Defibrillator Model 4000, Product Number 10A0988-A01.    The LifeVest system is indicated for patients 18 years of age and older who are at risk for sudden cardiac arrest and are not candidates for or refuse an implantable defibrillator.",
      "product_quantity": "33,670 units",
      "reason_for_recall": "Incorrect service code for properly catching critical defects during self-check. Potential for defibrillation shock failure",
      "recall_initiation_date": "20170912",
      "center_classification_date": "20180114",
      "termination_date": "20210810",
      "report_date": "20180124",
      "code_info": "All Serial Numbers"
    }
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}