{
  "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": "Research Triangle Park",
      "address_1": "2917 Weck Dr.",
      "reason_for_recall": "The product did not meet minimum and/or average minimum Teleflex resorption strength requirements.",
      "address_2": "",
      "product_quantity": "7,380 ea (total)",
      "code_info": "Product Code: 200101-01, Lot # 02F0801290 and  Product Code: BP1000V2L, Lot numbers: 02C1003535 & 02F1000711.",
      "center_classification_date": "20140501",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of CA, CO, GA, LA, IL, MA, MI, MN, MO, NC, and in the countries of Ireland and Singapore.",
      "state": "NC",
      "product_description": "Dekna-lok, 1 x 17.78 cm, Violet Braided Polyglycolic Acid Coated Suture, Synthetic Absorbable Surgical Suture USP, Rx Only, Sterile. Teleflex Product Code: 200101-01.",
      "report_date": "20140507",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Teleflex Medical",
      "recall_number": "Z-1535-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67973",
      "termination_date": "20160329",
      "more_code_info": "",
      "recall_initiation_date": "20140311",
      "postal_code": "27709",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}