{
  "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": "84598",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide and Foreign: countries of Canada, CHINA, NETHERLANDS",
      "recall_number": "Z-0871-2020",
      "product_description": "ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp  Mode Number: 110032332    Product Usage:  The device is a general orthopedic manual surgical instrument",
      "product_quantity": "67 units",
      "reason_for_recall": "Potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broach",
      "recall_initiation_date": "20191219",
      "center_classification_date": "20200128",
      "termination_date": "20200811",
      "report_date": "20200205",
      "code_info": "Lot Numbers: 827310, 711160, 203240"
    }
  ]
}