{
  "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": "Andover",
      "address_1": "3000 Minuteman Road",
      "reason_for_recall": "Device may fail to deliver defibrillation therapy in either Manual Defib or AED mode.",
      "address_2": "",
      "product_quantity": "64972",
      "code_info": "Serial numbers ranging from US00100100 to US00565942    Product Codes:  M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6",
      "center_classification_date": "20130429",
      "distribution_pattern": "Worldwide distribution:  USA (nationwide) and countries of: Afghanistan, Albania, Argentina, Australia, Austria,  Azerbaijan, Bahrain, Bangladesh, Belgium, Bolivia, Bosnia and Herzegowina, Brazil, Brunei Darussalam, Bulgaria, Canada, Cambodia, Chile, China, Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark, Ecuador, Egypt, El Salvador, Estonia, Ethiopia, Finland, France, Germany, Greece, Guadeloupe, Hong Kong, Iceland, India, Indonesia, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, Republic Of, Kuwait, Laos, Latvia, Lebanon, Libyan Arab Jamahiriya, Lithuania, Luxembourg, Macau, Macedonia, Malaysia, Malta, Mexico, Mongolia, Morocco, Namibia, Nepal, Netherlands (Antilles), New Caledonia, New Zealand, Nicaragua, Nigera, Norway, Oman, Pakistan, Palestine, Panama, Papua New Guinea, Paraguay, Peru, Philippines, Poland, Portugal, Puerto, Rico, Qatar, Reunion, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovenia, South Africa, Spain, SRI Lanka, Sweden, Switzerland, Taiwan (Province of China), Tanzania, Thailand, Trinidad and Tobago, Tunisia, Turkey, Turkmenistan, Uganda, Ukraine, United Arab Emirates, United Kingdom, Uzbekistan, Venezuela, Veit Nam, and Yemen.",
      "state": "MA",
      "product_description": "HeartStart MRx Monitor/Defribillator; Product Codes:  M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6.      The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation.",
      "report_date": "20130508",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Healthcare Inc.",
      "recall_number": "Z-1189-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64860",
      "termination_date": "20170110",
      "more_code_info": "",
      "recall_initiation_date": "20130408",
      "postal_code": "01810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}