{
  "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": "San Jose",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78668",
      "recalling_firm": "Stryker Corporation",
      "address_1": "5900 Optical Ct",
      "address_2": "N/A",
      "postal_code": "95138-1400",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed domestically to .      Distributed internationally to Australia and Mexico.",
      "recall_number": "Z-0837-2018",
      "product_description": "STRYKER WEDGE INTERFERENCE SCREW SYSTEM, ACL Interface Screw, 9MM X 25MM, Model 0234010056, labeled sterile.",
      "product_quantity": "60,753 units total",
      "reason_for_recall": "Routine bioburden testing of certain lots were found to have levels higher than internal acceptable rates.",
      "recall_initiation_date": "20171117",
      "center_classification_date": "20180302",
      "termination_date": "20240129",
      "report_date": "20180314",
      "code_info": "Model 0234010056, UDI 04546540754561,  Lot No. 17278AG2"
    }
  ]
}