{
  "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": "2026-08-20",
    "results": {
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      "product_res_number": "Z-0339-06",
      "event_date_initiated": "2005-09-08",
      "event_date_posted": "2006-01-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-03-07",
      "res_event_number": "33451",
      "product_code": "GWM",
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      "code_info": "W050708, W050980, & W050997",
      "firm_fei_number": "2023988",
      "recalling_firm": "Integra Neuro Sciences",
      "address_1": "5955 Pacific Center Blvd",
      "city": "San Diego",
      "state": "CA",
      "postal_code": "92121-4309",
      "additional_info_contact": "Eduardo Blanco\n858-455-1115 Ext. 115",
      "reason_for_recall": "Certain Model NS-P probes contained in the NeuroSensor Cerebral Blood Flow and Intracranial Pressure Monitoring Kit may allow an Intracranial Pressure (ICP) drift of up to  5 mmHg during the first 24 hours of monitoring ICP.  This is outside the products labeling specification of  2 mmHg maximum ICP drift within the first 24 hours of monitoring.",
      "root_cause_description": "Other",
      "action": "Notify Customers and Sales Representatives who received the product by letter sent via Federal Express. Customers will be instructed that an Integra Sales Representative will contact them to arrange for return of affected product.",
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