{
  "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": "Oak Creek",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82719",
      "recalling_firm": "Ad-Tech Medical Instrument Corporation",
      "address_1": "400 W Oakview Pkwy",
      "address_2": "N/A",
      "postal_code": "53154-7213",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - Nationwide distribution in the state of Illinois  and countries of Russia and United Kingdom",
      "recall_number": "Z-2396-2019",
      "product_description": "AD-TECH Spencer Probe Depth Electrode    Product Usage:  The Ad-Tech Depth Electrodes (Depth Electrodes, Foramen Ovale Depth Electrodes, Macro Micro Depth Electrodes, Spencer Probe Depth Electrodes, Wyler Sphenoidal Depth Electrodes) are intended for temporary (< 30 days) use with recording, monitoring and stimulation equipment for the recording, monitoring and stimulation of electrical signals at the subsurface level of the brain. The recording of electrical activity supports definition of the location of epileptogenic foci and brain mapping.",
      "product_quantity": "18",
      "reason_for_recall": "An Ad-Tech Clinical Specialist, attended a case on April 15, 2019. During the case the surgeon encountered an issue  after implanting four Ad-Tech depth electrodes. Upon initial device testing subsequent to implantation it was identified  that two of the devices that were labeled as 8 contact depth electrodes (SD08R-SP05X-000) were in fact 6 contact  depth electrodes (SD06R-SP05X-000) . There was no impact to the patient due to this incident.",
      "recall_initiation_date": "20190416",
      "center_classification_date": "20190826",
      "termination_date": "20220527",
      "report_date": "20190904",
      "code_info": "Catalog Numbers  SD08R-SP05X-000  SD06R-SP05X-000    LOT NUMBERS  127219 208140699  127357 208140699"
    }
  ]
}