{
  "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,
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    }
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  "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-0083-2021",
      "product_description": "Biomet ONPOINT SCOPE PROCEDURE KIT-EU  Item Number: 24-3055",
      "product_quantity": "US: 33 units; OUS:\t269 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",
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