{
  "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-2511-2021",
      "product_description": "Univation X System knee implant devices as  follows:  Catalog/Product:  NL482 UNIVATION F MENISCAL COMP.T1 RM/LM 9MM;  NL483 UNIVATION F MENISCAL COMP.T2 RM/LM 9MM;  NL484 UNIVATION F MENISCAL COMP.T3 RM/LM 9MM;  NL485 UNIVATION F MENISCAL COMP.T4 RM/LM 9MM;  NL486 UNIVATION F MENISCAL COMP.T5 RM/LM 9MM;  NL487 UNIVATION F MENISCAL COMP.T6 RM/LM 9MM",
      "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": ""
    }
  ]
}