{
  "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": "2026-07-01",
    "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": "98340",
      "recalling_firm": "Encore Medical, LP",
      "address_1": "9800 Metric Blvd",
      "address_2": "N/A",
      "postal_code": "78758-5445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of VA, TN, IL, IN, MI, CO, WY, MT, RI, MA, NJ, PA, MO, OK, LA, FL, CA.",
      "recall_number": "Z-1458-2026",
      "product_description": "Brand Name: Reverse Shoulder Prosthesis (RSP)  Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus  Model/Catalog Number: 509-00-432",
      "product_quantity": "20 implants",
      "reason_for_recall": "Knee and Humeral socket implants contain incorrect labeling.",
      "recall_initiation_date": "20260115",
      "center_classification_date": "20260224",
      "report_date": "20260304",
      "code_info": "Lot Code: Lot: 385P1263 GTIN: 00888912144575"
    }
  ]
}