{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Mahwah",
      "address_1": "325 Corporate Dr",
      "reason_for_recall": "Stryker has received a report which identified that a Triathlon Tibial Bearing Insert CS X3 Size #2 9mm (5531-G-209) was reported to be in a pack that was labelled as a CR insert (5530-G-209).",
      "address_2": "",
      "product_quantity": "10 units",
      "code_info": "Catalog number 5530-G-209     Lot Code LEF064",
      "center_classification_date": "20150814",
      "distribution_pattern": "OH, SC, RI, WV",
      "state": "NJ",
      "product_description": "Stryker Orthopaedics Triathlon X3 Tibial Bearing Insert - CR  REF 5530-G-209 (component of the Triathlon Total Knee System) for fixation to the tibial baseplates via a locking wire mechanism.",
      "report_date": "20150826",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Howmedica Osteonics Corp.",
      "recall_number": "Z-2389-2015",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "71678",
      "termination_date": "20160926",
      "more_code_info": "",
      "recall_initiation_date": "20150529",
      "postal_code": "07430-2006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}