{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Nazerat Illit",
      "state": "N/A",
      "country": "Israel",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82540",
      "recalling_firm": "Alpha Omega Engineering",
      "address_1": "PO Box 810, Haavoda Street",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US nationwide distribution: AL, AZ, CA, CO, GA, IL, LA, MD, MA, MI, MN, OH, PA, RI, TX, and VA",
      "recall_number": "Z-1216-2019",
      "product_description": "Neuro Omega System, incorporating HaGuide software.    For neurological and neurosurgical use.     To monitor, record and display bioelectric signals, and stimulate nerves and brain tissue.",
      "product_quantity": "29",
      "reason_for_recall": "If cables are improperly connected, current may reach high charge density, causing tissue harm.",
      "recall_initiation_date": "20180904",
      "center_classification_date": "20190506",
      "termination_date": "20201103",
      "report_date": "20190515",
      "code_info": "Serial numbers: 113, 115, 116, 118, 123, 121, 125, 129, 130, 137, 138, 141, 140, 146, 149, 147, 156/04, 159/04, 163/04, 161/04, 167, 175/06, 176/06, 177/06, 180/06, 182/06, 185/06, 188/06, and 189."
    }
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}