{
  "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": [
    {
      "country": "United States",
      "city": "Plainsboro",
      "address_1": "311 Enterprise Dr",
      "reason_for_recall": "Stability did not meet acceptance criteria for visual appearance during mixing and force vs. displacement at 6 months",
      "address_2": "",
      "product_quantity": "274 units",
      "code_info": "Lot Code: 2991332",
      "center_classification_date": "20190515",
      "distribution_pattern": "Worldwide Distribution - US Nationwide  Foreign; Peru, Ecuador, Columbia, Brazil",
      "state": "NJ",
      "product_description": "Integra Flowable Wound Matrix  Catalog No: FWD301    Product Usage:  Integra Flowable Wound Matrix is indicated for the treatment of tunneling and/or undermined wounds including: surgical wounds (donor sites/grafts, post-Moh s surgery, post-laser surgery, podiatric, wound dehiscence) and diabetic ulcers of both partial and full-thickness varieties. The device is intended for one-time use.",
      "report_date": "20190522",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Integra Limited",
      "recall_number": "Z-1338-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82653",
      "termination_date": "20200507",
      "more_code_info": "",
      "recall_initiation_date": "20190331",
      "postal_code": "08536-3344",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}