{
  "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": [
    {
      "country": "United States",
      "city": "Racine",
      "address_1": "1901 William St",
      "reason_for_recall": "The recall has been initiated due to concerns that the applicator wand may malfunction potentially causing the inability to monitor the VII cranial nerve. .",
      "address_2": "",
      "product_quantity": "13 kits (26 electrodes, 26 applicator wands, 26 leadwires).",
      "code_info": "Lot number 208140447  Batch Number 0060002;   Lot Number 208140458  Batch Number 0061723;  LotNumber208140487R Batch Number 0067938.",
      "center_classification_date": "20141021",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) in the states of: CO, FL, LA, NJ, OH, WA, and WI; and internationally to: Finland.",
      "state": "WI",
      "product_description": "Box Label: 3 mm Cueva Electrode Kit, Sterile EO, Rx Only, REF. CNE1-3KDINX .  Pouch labels: Each kit contains 3 pouches. 3 mm Cueva Electrode CNE-3X, Cueva Electrode Applicator Wand CNE-100X, Cueva Electrode Leadwire CNE-LW-2DINX.    Box Label: 2 mm Cueva Electrode Kit, Sterile EO, Rx Only, REF. CNE1-2KDINX .  Pouch labels: Each kit contains 3 pouches. 3 mm Cueva Electrode CNE-2X, Cueva Electrode Applicator Wand CNE-100X, Cueva Electrode Leadwire CNE-LW-2DINX.",
      "report_date": "20141029",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ad-Tech Medical Instrument Corporation",
      "recall_number": "Z-0106-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69436",
      "termination_date": "20150408",
      "more_code_info": "",
      "recall_initiation_date": "20141008",
      "postal_code": "53404-1876",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}