{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96348",
      "recalling_firm": "Zimmer, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1329-2025",
      "product_description": "Z1 Femoral Hip System, Product Number 611777612",
      "product_quantity": "35 units",
      "reason_for_recall": "There is a potential design issue with the Z1 Offset Stem Inserter leading to fracturing of the distal tip.",
      "recall_initiation_date": "20250212",
      "center_classification_date": "20250313",
      "report_date": "20250319",
      "code_info": "UDI-DI: 00887868577888; Lot Numbers: 102646 102777 102778 104095 104324 105277",
      "more_code_info": ""
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}