{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Plainsboro",
      "address_1": "105 Morgan Ln",
      "reason_for_recall": "Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.",
      "address_2": "",
      "product_quantity": "4, 799 boxes",
      "code_info": "1125682, 1125681  1125817, 1125983, 1126018  1126019, 1130641  1130642, 1110848, 1110849  1111883, 1111354, 1111884  1111936, 1112151  1110256, 1111355",
      "center_classification_date": "20130510",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) including Puerto Rico and countries of: Arab Emirates, Argentina, Belgium, Brasil, Canada, Chile, China, Costa Rica, Denmark, Egypt, Spain, France, Great Britain, Italy, Japan, Peru, Singapore, Thailand, and South Africa.",
      "state": "NJ",
      "product_description": "Suturable DuraGen Dural Regenerative Matrix    Suturable DuraGen Dural Regenerative Matrix is an absorbable implant for repair of dural defects. Suturable DuraGen is an easy to handle, soft, white, pliable, nonfriable, porous collagen matrix with a mechanically strengthened collagen component. Suturable DuraGen is supplied sterile, non-pyrogenic, for single use in double peel packages in a variety of sizes. Suturable DuraGen may be applied using either on-lay or suturing techniques depending on clinical need and surgeon preference.",
      "report_date": "20130522",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Integra LifeSciences Corporation",
      "recall_number": "Z-1283-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64778",
      "termination_date": "20150603",
      "more_code_info": "",
      "recall_initiation_date": "20130328",
      "postal_code": "08536-3339",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}