{
  "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": "Framingham",
      "address_1": "111 Lawrence St",
      "reason_for_recall": "A programing error in some Model FD100 HomeSafe AutoAlert Pendants will render the fall detection feature  inoperable.",
      "address_2": "",
      "product_quantity": "20201",
      "code_info": "Model FD100 HomeSafe AutoAlert Pendants with  Reference Number 300000219841 and 300000219851    All materials with R and UR prefixes remanufactured between 07-28 -2017 and 1 1-06-20 17; 100% of this material (UDI) are affected.",
      "center_classification_date": "20180406",
      "distribution_pattern": "US and Canada distribution",
      "state": "MA",
      "product_description": "HomeSafe AutoAlert Pendant works in conjunction with a compatible Lifeline communicator.",
      "report_date": "20180418",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Lifeline Systems Company",
      "recall_number": "Z-1316-2018",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "79010",
      "termination_date": "20190516",
      "more_code_info": "",
      "recall_initiation_date": "20171113",
      "postal_code": "01702-8156",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}