{
  "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": "Prairie Du Sac",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85884",
      "recalling_firm": "Mueller Sports Medicine, Inc",
      "address_1": "1 Quench Dr",
      "address_2": "N/A",
      "postal_code": "53578-2100",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. distribution only: AR and OH.",
      "recall_number": "Z-2475-2020",
      "product_description": "Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box",
      "product_quantity": "135,354 units",
      "reason_for_recall": "Natural rubber is present in Hybrid Wraparound Knee Support labeled as \"Not made with Natural Rubber latex\".",
      "recall_initiation_date": "20200618",
      "center_classification_date": "20200630",
      "termination_date": "20211029",
      "report_date": "20200708",
      "code_info": "Reference number: 64217, UPC number: 074676642178"
    }
  ]
}