{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86261",
      "recalling_firm": "Exactech, Inc.",
      "address_1": "2320 NW 66th Ct",
      "address_2": "N/A",
      "postal_code": "32653-1630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic: CO,FL,OK, PA.   International: Chile",
      "recall_number": "Z-2926-2020",
      "product_description": "The Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm.",
      "product_quantity": "11 units",
      "reason_for_recall": "The Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm,  were found to have a labeling error. Exactech is recalling the Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm because they were found to have a labeling error.  The upper right corner of the label incorrectly identifies the implant size as 3 when the implant size is 4.",
      "recall_initiation_date": "20200810",
      "center_classification_date": "20200831",
      "report_date": "20200909",
      "code_info": "Catalog Number: 350-22-44  Lot numbers: 05144883 and 05144884  Serial Numbers:  6417984, 6417989, 6417996, 6417997, 6417998, 6418002, 6418003, 6488668, 6488673,6488674,6488675."
    }
  ]
}