{
  "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": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "The potential that the end of the shaft could fail to effectively mate with the broach with the Calcar Planar Shaft instrument, part number 110032331.",
      "address_2": "",
      "product_quantity": "73",
      "code_info": "Model Number: 11032331  Lots: 784060, 662870",
      "center_classification_date": "20191122",
      "distribution_pattern": "CA, IN, MN, NJ, NY, AR, LA, OH, KY, TX, CO (US)  CA, CN, NL (International)",
      "state": "IN",
      "product_description": "ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331",
      "report_date": "20191204",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0517-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "84124",
      "termination_date": "20200824",
      "more_code_info": "",
      "recall_initiation_date": "20190806",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}