{
  "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,
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  },
  "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-0307-2020",
      "product_description": "Periarticular Plates - Tibial, Item Nos. 00234700304  00234700306  00234700308  00234700310  00234700312  00234700314  00234700316  00234700404  00234700406  00234700408  00234700410  00234700412  00234700414  00234700416  00234700502  00234700504  00234700506  00234700508  00234700510  00234700512  00234700514  00234700602  00234700604  00234700606  00234700608  00234700610  00234700612  00234700614  00234700704  00234700706  00234700708  00234700710  00234700712  00234700714  00234700716  00234700718  00234700720  00234700804  00234700806  00234700808  00234700810  00234700812  00234700814  00234700816  00234700818  00234700820  00234700904  00234700906  00234700908  00234700910  00234700912  00234700914  00234700916  00234700918  00234700920  00234701004  00234701006  00234701008  00234701010  00234701012  00234701014  00234701016  00234701018  00234701020  00234701104  00234701106  00234701108  00234701110  00234701204  00234701206  00234701208  00234701210  00234701304  00234701306  00234701308  00234701404  00234701406  00234701408  00234703500  00234703600",
      "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 product manufactured prior to January 2014."
    }
  ]
}