{
  "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": "Ongoing",
      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95951",
      "recalling_firm": "Integra LifeSciences Corp.",
      "address_1": "1100 Campus Rd",
      "address_2": "",
      "postal_code": "08540-6650",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of FL, NC, MA, MN, OH, DC, VA, CA, WI, NE, TX, NY, MI, OR, NJ, SC, AZ, UT, RI, IN, GA, CO and the countries of Canada, Australia, New Zealand, Cyprus, Sweden, Finland, Slovenia and Great Britain.",
      "recall_number": "Z-0977-2025",
      "product_description": "CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810    Implantable device that provides constant intraventricular pressure and drainage of CSF for the management of hydrocephalus.",
      "product_quantity": "132 units",
      "reason_for_recall": "Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.",
      "recall_initiation_date": "20241216",
      "center_classification_date": "20250117",
      "report_date": "20250129",
      "code_info": "UDI-DI: 10381780535874. Lot Numbers: 7432470, 7434917, 7434918 and 7438322.",
      "more_code_info": ""
    }
  ]
}