{
  "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": [
    {
      "country": "United States",
      "city": "Research Triangle Park",
      "address_1": "2917 Weck Dr",
      "reason_for_recall": "The device\u0019s wings may become partially detached from the EFx Shield during use.",
      "address_2": "",
      "product_quantity": "2265 units",
      "code_info": "Product Code: EFX002, Lot numbers: 3264480000, 3269990000, 3270100000.",
      "center_classification_date": "20161214",
      "distribution_pattern": "Domestic; US Nationwide; International: Belgium, Canada.",
      "state": "NC",
      "product_description": "Weck Facial  Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing incision sites.",
      "report_date": "20161221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Teleflex Medical",
      "recall_number": "Z-0759-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75693",
      "termination_date": "20171213",
      "more_code_info": "",
      "recall_initiation_date": "20161116",
      "postal_code": "27709-0186",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}