{
  "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": "Freiburg Im Breisgau",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89458",
      "recalling_firm": "Stryker Leibinger GmbH & Co. KG",
      "address_1": "Botzinger Str. 41",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide.",
      "recall_number": "Z-0715-2022",
      "product_description": "MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032",
      "product_quantity": "74",
      "reason_for_recall": "Inside the packaging of one reported item a non-conforming product was found. Contrary to the design, the barrier layer was manufactured on the inferior side of the implant versus the superior side.",
      "recall_initiation_date": "20211229",
      "center_classification_date": "20220303",
      "termination_date": "20231221",
      "report_date": "20220309",
      "code_info": "UDI: 07613252084334;  Lot Number: 3R7YHD",
      "more_code_info": ""
    }
  ]
}