{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sunnyvale",
      "address_1": "650 Almanor Ave",
      "reason_for_recall": "Complaints associated with an unexpected stop in AutoPulse compressions.",
      "address_2": "",
      "product_quantity": "3881 in US, 1846 ROW.",
      "code_info": "all",
      "center_classification_date": "20130109",
      "distribution_pattern": "Worldwide distribution.",
      "state": "CA",
      "product_description": "AutoPulse Resuscitation System Model 100,    Mfg by:Zoll Circulation  Sunnyvale, CA.    The AutoPulse Model 100 Automatic Mechanical Chest compressor is intended to be used as an adjunct to manual CPR, on adult patients only, in cases of clinical death as defined by lack of spontaneous breathing and pulse.",
      "report_date": "20130116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zoll Circulation, Inc.",
      "recall_number": "Z-0658-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62950",
      "termination_date": "20140512",
      "more_code_info": "",
      "recall_initiation_date": "20120808",
      "postal_code": "94085-3513",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}