{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "210155",
      "product_res_number": "Z-0219-2025",
      "event_date_initiated": "2024-09-19",
      "event_date_posted": "2024-10-24",
      "recall_status": "Completed",
      "res_event_number": "95414",
      "product_code": "GZL",
      "k_numbers": [
        "K163355"
      ],
      "product_description": "AD-TECH Spencer Probe Depth Electrode, REF SD04R-AP58X-000 4-Contact 1.12mm (A style) Depth Electrode",
      "code_info": "UDI/DI 00841823107510,  Lot Number 170052 858859860",
      "firm_fei_number": "2183456",
      "recalling_firm": "Ad-Tech Medical Instrument Corporation",
      "address_1": "400 W Oakview Pkwy",
      "city": "Oak Creek",
      "state": "WI",
      "postal_code": "53154-7213",
      "additional_info_contact": "Frederick Guesneau\n262-634-1555 Ext. 3000",
      "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.",
      "root_cause_description": "Employee error",
      "action": "AD-TECH issued an URGENT:  MEDICAL DEVICE RECALL notice to its consignees on 09/19/2024.  The notice explained the problem with the devices, risk to health, and requested the consignee contact customer support to obtain an RMA to expedite the return of the affected product.  \nFor questions:  contact your Ad-Tech Clinical Specialist.",
      "product_quantity": "2 units",
      "distribution_pattern": "US Nationwide distribution in the states of CA, OH.",
      "openfda": {
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        "registration_number": [
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        "device_name": "Electrode, Depth",
        "medical_specialty_description": "Neurology",
        "regulation_number": "882.1330",
        "device_class": "2"
      }
    }
  ]
}