{
  "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 Rd",
      "reason_for_recall": "Error in the printing of the therapy energy setting labels on Philips HeartStart M3536A MRx Monitor/Defibrillators.   The first energy setting is labeled 10 when it should be labeled\u001c1-10",
      "address_2": "",
      "product_quantity": "93 units",
      "code_info": "Serial numbers:  US00558442 - US00558461 US00561519  US00558531 - US00558532 US00561578  US00558615                      US00562454  US00558758 - US00558759 US00562504 - US00562527  US00560165 - US00560166 US00562640 - US00562641  US00560738 - US00560739 US00562832  US00560740 - US00560745 US00563125  US00560872                      US00563231 - US00563243  US00560909                      US00564032  US00561068                      US00564177  US00561209                      US00564409  US00561447 - US00561452 US00564793",
      "center_classification_date": "20131227",
      "distribution_pattern": "Worldwide Distribution - US Distribution including the states of IN, MS, TX and VA., and the countries of DENMARK, FRANCE, GERMANY, SPAIN and SWITZERLAND.",
      "state": "MA",
      "product_description": "Philips HeartStart MRx Monitor/Defibrillator  Models: M3536A Options A20 - A27, HeartStart MRx ALS  Monitor (Grey)    The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician",
      "report_date": "20140108",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems, Inc.",
      "recall_number": "Z-0593-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67052",
      "termination_date": "20170322",
      "more_code_info": "",
      "recall_initiation_date": "20130607",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}