{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "cfres_id": "112116",
      "product_res_number": "Z-0658-2013",
      "event_date_initiated": "2012-08-08",
      "event_date_posted": "2013-01-09",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-05-12",
      "res_event_number": "62950",
      "product_code": "DRM",
      "k_numbers": [
        "K011046",
        "K022345",
        "K032852",
        "K040453",
        "K063602"
      ],
      "product_description": "AutoPulse Resuscitation System Model 100,\r\n\r\nMfg by:Zoll Circulation\r\nSunnyvale, CA.\r\n\r\nThe 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.",
      "code_info": "all",
      "firm_fei_number": "3003793491",
      "recalling_firm": "Zoll Circulation, Inc.",
      "address_1": "650 Almanor Ave",
      "city": "Sunnyvale",
      "state": "CA",
      "postal_code": "94085-3513",
      "additional_info_contact": "Sam Nanavati\n408-419-1030",
      "reason_for_recall": "Complaints associated with an unexpected stop in AutoPulse compressions.",
      "root_cause_description": "Employee error",
      "action": "Zoll sent Customer Notification letters dated August 8, 2012 to all affected customers.  The letter identified the product, problem, and actions to be taken by the customers.  Contact Zoll Technical Support Line at 1 (800) 348-9011 for further assistance.",
      "product_quantity": "3881 in US, 1846 ROW.",
      "distribution_pattern": "Worldwide distribution.",
      "openfda": {
        "k_number": [
          "K141809",
          "K833879",
          "K063602",
          "K811987",
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        ],
        "registration_number": [
          "3013964848",
          "3010617000",
          "3005445717",
          "3008727520",
          "3007275459",
          "3029871637",
          "3012972516",
          "1821850",
          "3026976873",
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        "fei_number": [
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          "3015876",
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        ],
        "device_name": "Compressor, Cardiac, External",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.5200",
        "device_class": "2"
      }
    }
  ]
}