{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Framingham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71208",
      "recalling_firm": "Lifeline Systems, Incorporated",
      "address_1": "111 Lawrence St",
      "address_2": "N/A",
      "postal_code": "01702-8156",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide Distribution including AK AZ CA CT FL IA IL KY MA MD MT NC NE NH NY OH OR SC VA WA and WI.",
      "recall_number": "Z-1987-2015",
      "product_description": "Philips GoSafe Communicator 7000L  Personal emergency response system.",
      "product_quantity": "3189 devices total, 38 are subject to recall",
      "reason_for_recall": "Home communicator Model 7000L may not sense the phone line under certain unusual landline phone conditions.",
      "recall_initiation_date": "20150422",
      "center_classification_date": "20150706",
      "termination_date": "20160824",
      "report_date": "20150715",
      "code_info": "Serial Numbers:  9030003931  9030001761  9030002025  9030002242  9030001588  9030000853  9030001696  9030003178  9030003086  9030000589  9030001526  9030003837  9030000681  9030003507  9030000600  9030001060  9030001517  9030004154  9030002875"
    }
  ]
}