{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91866",
      "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": "US Distribution to states of:  AZ, FL, GA, MI, NE, and TX.",
      "recall_number": "Z-1284-2023",
      "product_description": "G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462",
      "product_quantity": "12 units",
      "reason_for_recall": "The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.",
      "recall_initiation_date": "20230206",
      "center_classification_date": "20230323",
      "report_date": "20230329",
      "code_info": "UDI: (01)00880304703506(17)321128(10)65731960; Lot Number: 65731960"
    }
  ]
}