{
  "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": "83314",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed to the following states in the USA: AZ, CA, DC, GA, IL, KY, LA, MA, MD, MN, NC, NJ, NM, OH,OK, OR, SC, TX.    Distributed to Japan and Netherlands.",
      "recall_number": "Z-2231-2019",
      "product_description": "Orthopedic Salvage System (OSS) Hybrid Poly Tibia  Item # 151810",
      "product_quantity": "29",
      "reason_for_recall": "Cleaning processes potentially being ineffective",
      "recall_initiation_date": "20190702",
      "center_classification_date": "20190809",
      "termination_date": "20210910",
      "report_date": "20190821",
      "code_info": "Lot # All lots expiring prior to 06/30/2024  Affected products were distributed between June 2016 and February 2019."
    }
  ]
}