{
  "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": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87684",
      "recalling_firm": "Stryker Leibinger GmbH & Co. KG",
      "address_1": "Botzinger Str. 41",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution and the countries of Germany, Italy, France, Australia, Japan.",
      "recall_number": "Z-1436-2021",
      "product_description": "DirectInject consists of a sterile dual paste system which is calcium phosphate based. Upon injection through the Mixer-Cannula, the two pastes form a cement paste which is moldable. The injected cement paste will harden under normal body conditions to form hydroxyapatite.",
      "product_quantity": "321 units",
      "reason_for_recall": "Inability for the user to inject the paste from the syringe into the target  location.",
      "recall_initiation_date": "20210401",
      "center_classification_date": "20210419",
      "termination_date": "20221219",
      "report_date": "20210428",
      "code_info": "Lot: DI20311,DI20307     Product Code (UDI): 07613327123265",
      "more_code_info": ""
    }
  ]
}