{
  "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": "97412",
      "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": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of AL, AZ, CA, CO, FL, HI, IA, IL, IN, KS, KY, LA, MD, \tME, NE, NJ, NY, OH, PR, RI, SC, TN, TX, UT, VA, WA, WI.",
      "recall_number": "Z-2547-2025",
      "product_description": "Brand Name: DJO SURGICAL  Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER BOSS DRILL, 6.5mm  Model/Catalog Number: 804-06-312  Product Description: Material: S.S., Non Sterile",
      "product_quantity": "907 units",
      "reason_for_recall": "Their is a potential that the reamer may  kick or bind up  during or immediately prior to use.",
      "recall_initiation_date": "20250718",
      "center_classification_date": "20250910",
      "report_date": "20250917",
      "code_info": "Lot Code: All Lots GTIN: 00190446843832"
    }
  ]
}