{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "Investigation determined that units supplied were missing the 4x21 degree helix angle.",
      "address_2": "",
      "product_quantity": "4",
      "code_info": "Catalog numbers: 32-481000   Lot Numbers: 615860, 765230    Catalog Number: 32-481001  Lot Number Identification: 121450, 392410, 765250, 974290",
      "center_classification_date": "20141006",
      "distribution_pattern": "International Distribution in the countries of Netherlands, Europe, the Middle East, and Asia.",
      "state": "IN",
      "product_description": "Compress Face Reamer    Product Usage:    Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement, tumor resections, revision of previously failed total joint arthroplasty, and trauma.",
      "report_date": "20141015",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomet, Inc.",
      "recall_number": "Z-0021-2015",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "69280",
      "termination_date": "20150714",
      "more_code_info": "",
      "recall_initiation_date": "20140917",
      "postal_code": "46581",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}