{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "37180",
      "product_res_number": "Z-0623-05",
      "event_date_initiated": "2005-01-21",
      "event_date_posted": "2005-03-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-07-13",
      "res_event_number": "31117",
      "product_code": "GMW",
      "product_description": "LICOX temperature probe, Model C8.B",
      "code_info": "Lot numbers: 160504 and 240604",
      "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": "Nancy A. Mathewson\n858-455-1115 Ext. 185",
      "reason_for_recall": "LICOX  Model C8.B temperature probes manufactured by GMS mbH, an Integra company, may exhibit progen (endotoxin) levels above the FDA limit of 2.15 endotoxin units per device. Elevated endotoxin levels may result in an increased patient risk of fever.",
      "root_cause_description": "Other",
      "action": "LICOX  Model C8.B temperature probes and LICOX IM3.ST Complete Brain IMC Probe Kits manufactured by GMS mbH, an Integra company, may exhibit pyrogen (endotoxin) levels above the FDA limit of 2.15 endotoxin units per device. Elevated endotoxin levels may result in an increased patient risk of fever.",
      "product_quantity": "19",
      "distribution_pattern": "LA, CA, CO, DC, DE, FL, GA, IL, IN, LA,  MA, MD, MI, MN, MT, NC, NE, NY, OH, OR, PA, SD,  TN, TX, VA",
      "openfda": {
        "device_name": "Test, Sorbent, Fta-Abs",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3830",
        "device_class": "2"
      }
    }
  ]
}