{
  "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": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79700",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "130 & 120 Forbes Blvd",
      "address_2": "N/A",
      "postal_code": "02048",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to accounts in 7 states: AZ, ME, NY, OH, PA, TN, and VT; and PR.",
      "recall_number": "Z-1536-2018",
      "product_description": "Smith & Nephew Whipknot Soft Tissue Cinch #5 Sutures. PN: 7211015",
      "product_quantity": "22",
      "reason_for_recall": "Packaging design is insufficient to prevent potential sterile barrier breach (pin hole) in Tyvek film of pouch. A limited number of previously recalled devices were inadvertently redistributed.",
      "recall_initiation_date": "20171211",
      "center_classification_date": "20180426",
      "termination_date": "20200921",
      "report_date": "20180502",
      "code_info": "Batch No. 50498479; 50526605; 50527117; 50553176; 50579348; 50581344; 50588245; 50590542; 50591919; 50592295 & 50603355"
    }
  ]
}