{
  "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": "Terminated",
      "city": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82487",
      "recalling_firm": "Matrix Surgical Holdings, LLC",
      "address_1": "4025 Welcome All Rd Sw Ste 120",
      "address_2": "N/A",
      "postal_code": "30349-1876",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of Florida and Massachusetts and countries of   Argentina, Chile, Colombia, Iran, Mexico, Norway, Taiwan, and Turkey.",
      "recall_number": "Z-1223-2019",
      "product_description": "OMNIPORE Surgical Implant   Petite Paranasal - Left - Product Usage: OmniPore Surgical Implants in block, sheet, and anatomical shapes are intended for nonweight bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. OmniPore Surgical Implants are also intended for the augmentation or restoration of contour in the craniomaxillofacial skeleton.",
      "product_quantity": "46",
      "reason_for_recall": "Product mislabeling.",
      "recall_initiation_date": "20190130",
      "center_classification_date": "20190426",
      "termination_date": "20200623",
      "report_date": "20190508",
      "code_info": "OP9519 / Lot # 00855421005864 021050617"
    }
  ]
}