{
  "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": "Lynge",
      "state": "",
      "country": "Denmark",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81085",
      "recalling_firm": "Widex A/S",
      "address_1": "Nymollevej 6",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution to states of: GA and NY.",
      "recall_number": "Z-0094-2019",
      "product_description": "Widex BABY hearing aid (referred to as BABY440), powered by zinc-air batteries size 10    Intended use: BABY440 is intended for, but not limited to, babies (0 to 3 years of age) to be used as air conduction amplification devices in everyday listening environments.",
      "product_quantity": "2",
      "reason_for_recall": "The reason for this field action is due to the mounting of a non-tamper-resistant (ordinary) battery drawer on some BABY440 hearing aids.  The correct battery drawer is tamper-resistant and require a special tool to open it.",
      "recall_initiation_date": "20180831",
      "center_classification_date": "20181010",
      "termination_date": "20181221",
      "report_date": "20181017",
      "code_info": "Serial numbers 024569 and 024550",
      "more_code_info": ""
    }
  ]
}