{
  "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-2512-2021",
      "product_description": "Univation X System knee implant devices as  follows:  Catalog/Product:  NL488 UNIVATION F MENISCAL COMP.T1 RM/LM 10MM;  NL489 UNIVATION F MENISCAL COMP.T2 RM/LM 10MM;  NL490 UNIVATION F MENISCAL COMP.T3 RM/LM 10MM;  NL491 UNIVATION F MENISCAL COMP.T4 RM/LM 10MM;  NL492 UNIVATION F MENISCAL COMP.T5 RM/LM 10MM;  NL493 UNIVATION F MENISCAL COMP.T6 RM/LM 10MM",
      "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": ""
    }
  ]
}