{
  "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": "Campbell",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70466",
      "recalling_firm": "Zipline Medical",
      "address_1": "747 Camden Ave Ste A",
      "address_2": "N/A",
      "postal_code": "95008-4147",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and the countries of Panama, Tehran, Ireland, Sweden, Japan, Hong Kong, Finland, Pakistan, Taiwan, Malaysia.",
      "recall_number": "Z-1235-2015",
      "product_description": "Zip 8M Wound Closure Device;  for wounds up to 8 cm in length;  Product number PS9080;  Rx only, Sterile    Indicated for use during and after skin incision procedures to approximate skin and hold together skin edges until healing can take place.",
      "product_quantity": "3109 devices, total all model numbers",
      "reason_for_recall": "The manufacturers seal may not be present on the Nylon pouch resulting in lack of assurance for sterility.",
      "recall_initiation_date": "20150205",
      "center_classification_date": "20150302",
      "termination_date": "20150410",
      "report_date": "20150311",
      "code_info": "Lot 1002750, Exp 2016-09"
    }
  ]
}