{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Somerville",
      "address_1": "US Highway 22 West",
      "reason_for_recall": "Ethicon is recalling EVARREST Fibrin Sealant Patch because the characters \"0-bad\" were printed in the expiration date field on the foil pouch labels of the Fibrin Patch units instead of the valid expiration date (2016-12-28).",
      "address_2": "",
      "product_quantity": "228 units",
      "code_info": "Product Code #EVT5024, Lot #U01F012A",
      "center_classification_date": "20160615",
      "distribution_pattern": "Nationwide Distribution",
      "state": "NJ",
      "product_description": "EVARREST Fibrin Sealant Patch, Manufactured by: Omrix Biopharmaceuticals, Ltd, Israel.    Indicated for use with manual compression as an adjunct to hemostasis for control of bleeding during adult liver surgery and soft tissue bleeding in adults when control of bleeding by standard surgical methods of hemostasis is ineffective or impractical.",
      "report_date": "20160622",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ethicon, Inc.",
      "recall_number": "Z-1996-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71372",
      "termination_date": "20170802",
      "more_code_info": "",
      "recall_initiation_date": "20160411",
      "postal_code": "08876",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}