{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83962",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed nationwide.",
      "recall_number": "Z-0327-2020",
      "product_description": "CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201  00223200202",
      "product_quantity": "5,459,583 total devices",
      "reason_for_recall": "Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).",
      "recall_initiation_date": "20191010",
      "center_classification_date": "20191107",
      "termination_date": "20200519",
      "report_date": "20191113",
      "code_info": "77001932  77001933  77001878  62176030  62112090  62146839"
    }
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}