{
  "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": "Piscataway",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67241",
      "recalling_firm": "Siemens Hearing Instruments, Inc",
      "address_1": "10 Constitution Ave",
      "address_2": "",
      "postal_code": "08855",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA Nationwide Distribution",
      "recall_number": "Z-0988-2014",
      "product_description": "Siemens Prisma 2K Hearing Aid    Product Usage:  A behind the ear (BTE) hearing aid developed for pediatric patients.",
      "product_quantity": "738 units",
      "reason_for_recall": "Siemens became aware of an issue where an infant or child could open the tamper resistant battery compartment of the Siemens Prisma 2K hearing aid under certain unintended use conditions.",
      "recall_initiation_date": "20050701",
      "center_classification_date": "20140218",
      "termination_date": "20170706",
      "report_date": "20140226",
      "code_info": "Part numbers  1) 7773182  2) 7244028  3) 8757374  4) 8747086  5) 10056937  6) 10056938",
      "more_code_info": ""
    }
  ]
}