{
  "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": [
    {
      "country": "United States",
      "city": "Mahwah",
      "address_1": "325 Corporate Dr",
      "reason_for_recall": "Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.",
      "address_2": "",
      "product_quantity": "10,537 units",
      "code_info": "Catalog #6541-2-609  All lot codes",
      "center_classification_date": "20130829",
      "distribution_pattern": "Nationwide Distribution",
      "state": "NJ",
      "product_description": "Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp extramedullary (EM) referencing instrument (Cat. No. 6541-2-609), for use in Total Knee Arthroplasty (TKA) when the surgeon elects to use Stryker's Triathlon Total Knee System in conjunction with EM referencing. Non-Sterile Instrument.",
      "report_date": "20130904",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Howmedica Osteonics Corp.",
      "recall_number": "Z-2130-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65902",
      "termination_date": "20160427",
      "more_code_info": "",
      "recall_initiation_date": "20130702",
      "postal_code": "07430-2002",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}