{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Center Valley",
      "address_1": "3773 Corporate Pkwy",
      "reason_for_recall": "The NS357R Vega PS Tibia Trial/Preparation Plateau size T4 may be incorrectly labeled.  If the incorrect size trial is used the potential risk is implantation of the incorrect implant size which may lead to injury of ligaments, pain and possible revision surgery.",
      "address_2": "",
      "product_quantity": "13 Units",
      "code_info": "The product is located in the Vega Tibia preparation Tray (NS803) in the Vega Instrument Set (ST0468).",
      "center_classification_date": "20180212",
      "distribution_pattern": "USA (nationwide)",
      "state": "PA",
      "product_description": "NS357R Vega PS Tibia Trial/Preparation Plateau size T4 (Component of the Vega Knee System Set #ST0468)    The affected part is provided in the Vega Knee System Set #ST0468. The Vega Knee System is used for reconstruction of the diseased knee joint.",
      "report_date": "20180221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Aesculap Implant Systems LLC",
      "recall_number": "Z-0591-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79042",
      "termination_date": "20180808",
      "more_code_info": "",
      "recall_initiation_date": "20170810",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}