{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71009",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed in the states of IN, MN, FL, and IL, and the countries of Argentina and Germany.",
      "recall_number": "Z-1575-2015",
      "product_description": "NexGen Augment; 5mm Distal Femoral Augment;Part number 00-5990-036-10.    Intended to be used in total knee arthroplasty when there is insufficient bone in the distal femur.",
      "product_quantity": "20 units",
      "reason_for_recall": "The affected lot is being recalled because it was packaged without the locking screw.  The locking screw packaged with the augment is used to fix the augment to the femoral component.  This has the potential to delay surgery",
      "recall_initiation_date": "20150402",
      "center_classification_date": "20150501",
      "termination_date": "20150923",
      "report_date": "20150513",
      "code_info": "Part #00-5990-036-10;   lot 62815809"
    }
  ]
}