{
  "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": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76701",
      "recalling_firm": "Greatbatch Medical",
      "address_1": "2300 Berkshire Ln N",
      "address_2": "N/A",
      "postal_code": "55441-4575",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "NY",
      "recall_number": "Z-2781-2017",
      "product_description": "ViaPeel PTFE Peelable Introducer 5FR, Part Number 10890-006",
      "product_quantity": "5,000 devices",
      "reason_for_recall": "Greatbatch received complaints with the ViaPeel Introducer Sheath 5FR, of handles detaching during use.",
      "recall_initiation_date": "20161111",
      "center_classification_date": "20170729",
      "termination_date": "20171103",
      "report_date": "20170809",
      "code_info": "Lot Number:  W3101005"
    }
  ]
}