{
  "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": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94555",
      "recalling_firm": "Smith & Nephew Inc",
      "address_1": "6409 E Holmes Rd",
      "address_2": "",
      "postal_code": "38141-8310",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International distribution to the countries of Australia, Germany, Japan, Portugal, and United Kingdom.",
      "recall_number": "Z-1901-2024",
      "product_description": "smith&nephew OXINIUM Femoral Head 12/14 Taper, REF 71343204, 32 MM OD +4, Sterile; and smith&nephew, 12/14 Taper, REF 71343604, 36 MM M / +4",
      "product_quantity": "23 packages",
      "reason_for_recall": "Packaging contained the incorrect size of femoral head from what was displayed on the label.",
      "recall_initiation_date": "20240424",
      "center_classification_date": "20240524",
      "report_date": "20240605",
      "code_info": "REF 71343204 - Batch #23FM03219, Exp. June 2033; REF 71343604 - Batch 23FM04184, Exp. June 2033.",
      "more_code_info": ""
    }
  ]
}