{
  "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-2906-2016",
      "product_description": "CUSA Dissectron Fingertip Laparoscopic Cannula, REF F75221, Sterile EO, Rx only, packaged in a Tyvek pouch and secondary packaged in Tyvek pouch, Five (5) sealed pouches are packaged in a cardboard box.   For use with CUSA DISSECTRON Hand pieces and Sontrodes",
      "product_quantity": "9",
      "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 F75221, Lot #0195486 with expiry 04/2021"
    }
  ]
}