{
  "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": [
    {
      "status": "Terminated",
      "city": "Durham",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69918",
      "recalling_firm": "Teleflex Medical",
      "address_1": "4024 Stirrup Creek Dr",
      "address_2": "N/A",
      "postal_code": "27703-9000",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US (nationwide) including the states of AL, CA, FL, DE, IA, IL, IN, KY, MA, MN, NC, NE, NJ, NY, NV, OH, OK, PA, TX, VA, VT, and WA.",
      "recall_number": "Z-0826-2015",
      "product_description": "WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips.    Weck Ligating Clips are intended for use in procedures involving vessels or anatomic structures for which the surgeon determines ligating clips are the best choice.",
      "product_quantity": "3180 units",
      "reason_for_recall": "The manufacturing dates and expiration dates were transposed on the Tyvek label.",
      "recall_initiation_date": "20141203",
      "center_classification_date": "20141217",
      "termination_date": "20171124",
      "report_date": "20141224",
      "code_info": "Product Code: 523300, Lot number: 01B1400034"
    }
  ]
}