{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96019",
      "recalling_firm": "Encore Medical, LP",
      "address_1": "9800 Metric Blvd",
      "address_2": "",
      "postal_code": "78758-5445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of VA, MN, TX, WI, IA, IL, IN, SC, NY, MD, CA, FL, AZ, WA.",
      "recall_number": "Z-0766-2025",
      "product_description": "EMPOWR 3D Knee Tibial Insert, 5R 16MM, VE, REF: 342-16-705;  EMPOWR 3D Knee Tibial Insert, 3R 14MM, VE, REF: 342-14-703",
      "product_quantity": "33",
      "reason_for_recall": "5R 16MM knee tibial insert package may contain knee tibial insert 3R 14MM and vice versa, which may cause surgical delay to get a new product.",
      "recall_initiation_date": "20241218",
      "center_classification_date": "20241226",
      "report_date": "20250101",
      "code_info": "REF/UDI-DI/Lot:  342-16-705/00888912167628/159T1086 342-14-703/00888912167505/137T1086",
      "more_code_info": ""
    }
  ]
}