{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Oak Creek",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95414",
      "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": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of CA, OH.",
      "recall_number": "Z-0221-2025",
      "product_description": "AD-TECH Spencer Probe Depth Electrode, REF SD08R-AP58X-000 8-Contact 1.12mm (A style) Depth Electrode",
      "product_quantity": "14 units",
      "reason_for_recall": "Ad-Tech is recalling these A-Style SD Depth Electrodes because a label discrepancy was identified on A style contact SD electrodes where the MR Conditional symbol was incorrectly placed instead of the MR Unsafe symbol. The A style contacts were not cleared for MR Conditional use. Our records indicate you have received one or more of the affected lots listed above.",
      "recall_initiation_date": "20240919",
      "center_classification_date": "20241024",
      "report_date": "20241030",
      "code_info": "UDI/DI 00841823107688,  Lot Number 168788 855856857, 172999 873874875R, 174915 879880881",
      "more_code_info": ""
    }
  ]
}