{
  "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": "Somerville",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79668",
      "recalling_firm": "Ethicon, Inc.",
      "address_1": "Us Highway 22 West",
      "address_2": "N/A",
      "postal_code": "08876",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The device was distributed to the following states: AK, AL, AR, AZ, CA, CO, FL, GA, IA, IL MD, MI, MN, MO, NC, ND, NJ, NV, NY, OH, PA, TN, TX, WA, WI, and WV.  The device was also distributed to Puerto Rico.",
      "recall_number": "Z-1534-2018",
      "product_description": "Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3), Product Code EVT45.  Accessory Tips for use only with EVICEL Fibrin Sealant (Human) Application Device.",
      "product_quantity": "738 devices (246 boxes of 3)",
      "reason_for_recall": "Products labeled for distribution outside the United States may have been distributed to customers in the United States.",
      "recall_initiation_date": "20180307",
      "center_classification_date": "20180426",
      "termination_date": "20190430",
      "report_date": "20180502",
      "code_info": "Lot 17-0102"
    }
  ]
}