{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Mahwah",
      "state": "NJ",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64308",
      "recalling_firm": "Stryker Howmedica Osteonics Corp.",
      "address_1": "325 Corporate Drive",
      "address_2": "N/A",
      "postal_code": "07430",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA Nationwide Distribution",
      "recall_number": "Z-1052-2013",
      "product_description": "ShapeMatch Cutting Guides    Product Usage:  The ShapeMatch Cutting Guides are intended to be used as patient-specific surgical instrumentation to assist in the positioning of total knee arthroplasty components intraoperatively and in guiding the marking of bone before cutting.",
      "product_quantity": "7868 units",
      "reason_for_recall": "With regards to ShapeMatch Cutting Guides using MRI Imaging, Stryker Orthopaedics  has become aware that there are potential issues associated with internal processes  for planning cases and producing ShapeMatch Cutting Guides.",
      "recall_initiation_date": "20121108",
      "center_classification_date": "20130412",
      "termination_date": "20210111",
      "report_date": "20130424",
      "code_info": "Catalog No: TR7100-L and TR7100-R  Lot Code: All"
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}