{
  "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": [
    {
      "status": "Terminated",
      "city": "Durham",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67711",
      "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": "Worldwide Distribution -- USA, including the states of AL, CA, FL, GA, IL, IN, KS, LA, ME, MA, MI, MN, MS, MO, NV, NJ, NM, NY, OH, PA, RI, SC, TN, TX, UT, VA, WV, and WI; and countries of Canada, Germany, and Ireland.",
      "recall_number": "Z-1555-2014",
      "product_description": "Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize,  Deknatel.    Indicated for use in soft tissue approximation.",
      "product_quantity": "32,271 ea.",
      "reason_for_recall": "Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.",
      "recall_initiation_date": "20140311",
      "center_classification_date": "20140506",
      "termination_date": "20170814",
      "report_date": "20140514",
      "code_info": "Product Code 1154654 -  Lot 02K0801212"
    }
  ]
}