{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mahwah",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67384",
      "recalling_firm": "Stryker Howmedica Osteonics Corp.",
      "address_1": "325 Corporate Dr",
      "address_2": "N/A",
      "postal_code": "07430-2002",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in PA.",
      "recall_number": "Z-0975-2014",
      "product_description": "Stryker CMF Customized Implant Kit X-Large; 5444-0-401 X-Large Implant (2)   5444-01-102 Host Bone; Howmedica Osteonics Corp.  325 Corporate Drive, Mahwah, NJ 07430 USA.    Designed individually for each patient to correct trauma and/or defects in mandibular, maxillofacial, or craniofacial bone.",
      "product_quantity": "one unit",
      "reason_for_recall": "Stryker received a report from the field that an incorrect patient-specific Simplex P CMF Customized Implant Kit was delivered to a hospital.",
      "recall_initiation_date": "20131206",
      "center_classification_date": "20140212",
      "termination_date": "20150506",
      "report_date": "20140219",
      "code_info": "510 K103010  Catalog # 5444-0-400  Lot Code K08702VR21FEB"
    }
  ]
}