{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Princeton",
      "address_1": "1100 Campus Rd",
      "reason_for_recall": "Nonconforming product which was dispositioned for rejection was mistakenly released for commercial use.",
      "address_2": "",
      "product_quantity": "55",
      "code_info": "Lot # 3388360",
      "center_classification_date": "20200311",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, IN, LA, MI, MN, MO, NC, NM, NY, PA, SC, and TX and countries of Italy, France, Germany, and Finland.",
      "state": "NJ",
      "product_description": "NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.",
      "report_date": "20200318",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Integra LifeSciences Corp.",
      "recall_number": "Z-1470-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84960",
      "termination_date": "20200610",
      "more_code_info": "",
      "recall_initiation_date": "20200207",
      "postal_code": "08540-6650",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}