{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Plainsboro",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83831",
      "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": "Visit",
      "distribution_pattern": "The products were distributed to the following US states:  CA, CO, CT, FL, IN, NY, OK, PA, TX, WI, and WV.  The products were distributed to the following foreign countries:  Australia, Belgium.",
      "recall_number": "Z-0124-2020",
      "product_description": "Cerelink ICP Monitor, Model Number 826820;  intended for use as an interface between compatible strain-gauge type pressure transducers and standard physiological pressure monitoring systems.",
      "product_quantity": "189",
      "reason_for_recall": "There is a potential for a progressive decline in observed ICP readings of the monitor during use.",
      "recall_initiation_date": "20190912",
      "center_classification_date": "20191012",
      "report_date": "20191023",
      "code_info": "All systems"
    }
  ]
}