{
  "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": "Terminated",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88325",
      "recalling_firm": "Aesculap Implant Systems LLC",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2516-2021",
      "product_description": "Univation X System Tray Sysem knee implant devices as  follows:  Tray Number/Set Name/Set Number  NM1090R Navigation Set ST0560;  NM1092R + NM1095R + NM1096R (Tray insert to NM1095R) univation XF ST0540;  NM1093R univation XF OPT ST0544",
      "product_quantity": "",
      "reason_for_recall": "Malfunction- loosening of the implant resulting in a potential revision surgery",
      "recall_initiation_date": "20210319",
      "center_classification_date": "20210922",
      "termination_date": "20250328",
      "report_date": "20210929",
      "code_info": "All lots",
      "more_code_info": ""
    }
  ]
}