{
  "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": "2026-04-15",
    "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": "75237",
      "recalling_firm": "Zimmer 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": "Worldwide Distribution - US Nationwide in the states of NJ, MI, FL and the countries of Sweden and Canada.",
      "recall_number": "Z-0111-2017",
      "product_description": "Vanguard Distal Femoral Augment 75 X 5 RL/LM    Product Usage:  \u001d Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved. \u001c Correction of varus, valgus, or posttraumatic deformity. \u001c Correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure. \u001c The device is a single use implant intended for implantation with bone cement.",
      "product_quantity": "5",
      "reason_for_recall": "Contents of the package do not match the product labeling.  Product is labeled: Vanguard Distal Femoral Augment 75 X 5 RL/LM  Carton contains: Vanguard Distal Femoral Augment 75 X 5 LL/RM  Risks:  Adverse health outcomes that could occur as a result of this event are a delay less than 30 minutes and a different size augment being used to complete the procedure.  As the augment will not assemble with femoral component due to its shape, it would be easily identified during surgery.",
      "recall_initiation_date": "20160809",
      "center_classification_date": "20161017",
      "termination_date": "20170517",
      "report_date": "20161026",
      "code_info": "Item Number  184108  Lot Number  183410  Exp. 8/27/2025"
    }
  ]
}