{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Brooklyn",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91982",
      "recalling_firm": "Fisher Wallace Laboratories Inc.",
      "address_1": "630 Flushing Ave Ste 104",
      "address_2": "N/A",
      "postal_code": "11206-5775",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide. Global Distribution.",
      "recall_number": "Z-1600-2023",
      "product_description": "Fisher Wallace Stimulator Models FW-100 and FW-200",
      "product_quantity": "43,489 total devices",
      "reason_for_recall": "If the batteries are installed incorrectly, the product may overheat, possibly leading to pain, discomfort, irritation, or even burns during use of the device.",
      "recall_initiation_date": "20230406",
      "center_classification_date": "20230517",
      "report_date": "20230524",
      "code_info": "FW-100: UDI-DI 00860000919005, Serial Numbers 2020200000-2022278000;  FW-200: UDI-DI 00860000919012, Serial Numbers 2021140129T-2022030528T"
    }
  ]
}