{
  "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-0334-2020",
      "product_description": "Metasul Taper Liner, various sizes, Item Nos. 00877000528  00877000628  00877000732  00877000832  00877000936  00877001036  00877001140  00877001240  00877001340  00877001440  00877001540  00877001640  00877001740  00877001840  00877001940  00877002040  00877002140  00877002240  00877002340",
      "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": "All products manufactured prior to January 2014."
    }
  ]
}