{
  "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-0838-2018",
      "product_description": "ACL DISPOSABLE PACK BONE-TENDON-BONE, Model 0234020280, 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.  It is indicated to be a single surgery use, disposable set of instrumentation for anterior cruciate ligament (ACL) reconstruction surgeries.",
      "recall_initiation_date": "20171117",
      "center_classification_date": "20180302",
      "termination_date": "20240129",
      "report_date": "20180314",
      "code_info": "Model 0234020280,  UDI 07613154643264,  Lot No. 17299AG2"
    }
  ]
}