{
  "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": [
    {
      "status": "Terminated",
      "city": "Eagan",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65423",
      "recalling_firm": "BRAEMAR, INC.",
      "address_1": "1285 Corporate Center Dr",
      "address_2": "N/A",
      "postal_code": "55121-1267",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide Distribution including FL, IL, MD, MN, NY, OH, PA, SC, TN, and TX.",
      "recall_number": "Z-1645-2013",
      "product_description": "Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-00 used with ER920 Wireless Series Arrhythmia Event Recorder.     Non-rechargeable disposable battery pack.",
      "product_quantity": "10,785 packs",
      "reason_for_recall": "Braemar Inc.,  became aware of a battery related incident that occurred with an Able battery pack being used in a Braemar ER920W wireless event monitor.  The event did not result in any patient related injury or present any clinical impact.",
      "recall_initiation_date": "20110502",
      "center_classification_date": "20130701",
      "termination_date": "20130715",
      "report_date": "20130710",
      "code_info": "n/a"
    }
  ]
}