{
  "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-2908-2016",
      "product_description": "Integra Drainage Accessory Kits, REF 910122, Sterile EO, Rx only, packaged in one Tyvek pouch. Five (5) sealed Tyvek pouches are packaged in a cardboard box.   Used for Intraoperative drainage of CSF",
      "product_quantity": "1",
      "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 910122, Lot #0195615 with expiry 04/2019"
    }
  ]
}