{
  "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": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99073",
      "recalling_firm": "Zimmer, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Refer to the attached ZFA 2026-00088_Initial Consignee List and ZFA 2026-00088_Initial Distribution History containing the distribution and the identification of the affected consignees.",
      "recall_number": "Z-2578-2026",
      "product_description": "Brand Name: Persona Revision  Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment  Model/Catalog Number: 42-5572-066-10  Software Version: N/A  Product Description: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Size 9, 9+ 10mm Thicknes  Component: N/A",
      "product_quantity": "12",
      "reason_for_recall": "Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.",
      "recall_initiation_date": "20260511",
      "center_classification_date": "20260624",
      "report_date": "20260701",
      "code_info": "Lot Code: Model No. 42-5572-066-10 ; UDI-DI (01)00889024561014(17)331103(10)66232947 ; Lot number 66232947"
    }
  ]
}