{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plainsboro",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75065",
      "recalling_firm": "Integra LifeSciences Corp.",
      "address_1": "311 Enterprise Dr",
      "address_2": "N/A",
      "postal_code": "08536-3344",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution to KS only",
      "recall_number": "Z-2909-2016",
      "product_description": "Integra Ventricular Catheter Accessory Kit, REF 951303, Sterile EO, Rx only, packaged in a PVC tray, then secondary package in to Tyvek pouch and tertiary packaged in to Tyvek pouch. Sealed pouches are packaged in a cardboard box.   F8 35cm Silicone Elastomer Ventricular Catheter for use with CSF external drainage systems",
      "product_quantity": "14",
      "reason_for_recall": "During final sampling inspection, one of the lots was discovered with a total incomplete packaging seal of the sterile product.",
      "recall_initiation_date": "20160823",
      "center_classification_date": "20160930",
      "termination_date": "20170329",
      "report_date": "20161012",
      "code_info": "Catalog Number 951303, Lot #0195786 with expiry 05/2019"
    }
  ]
}