{
  "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": "86424",
      "recalling_firm": "Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign: Canada,  FINLAND, NETHERLANDS, UNITED KINGDOM",
      "recall_number": "Z-0081-2021",
      "product_description": "Biomet Regenerex Primary Taper Cap  Item Number 141269",
      "product_quantity": "US: 62 units; OUS:\t176 units",
      "reason_for_recall": "Product not properly being aligned with the adequate gamma sterilization group and  result in the product not being properly sterilized",
      "recall_initiation_date": "20200904",
      "center_classification_date": "20201008",
      "termination_date": "20210831",
      "report_date": "20201014",
      "code_info": "Lot Numbers:  015800  324440  685300  023900  324440R  696280  058930  389060  821980  200720  418430  890320  313260  646040  997610"
    }
  ]
}