{
  "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": [
    {
      "status": "Terminated",
      "city": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75502",
      "recalling_firm": "Synthes (USA) Products LLC",
      "address_1": "1301 Goshen Pkwy",
      "address_2": "N/A",
      "postal_code": "19380-5986",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed Nationwide",
      "recall_number": "Z-0643-2017",
      "product_description": "2.5 mm TI Calibrated Reaming Rod 850 mm, Sterile",
      "product_quantity": "260 units",
      "reason_for_recall": "The peel pouches for the affected reaming rods and extraction hooks are delaminating.",
      "recall_initiation_date": "20161003",
      "center_classification_date": "20161119",
      "termination_date": "20170706",
      "report_date": "20161130",
      "code_info": "Catalog ID 359.083S, Lot Numbers: H115566; H116597; H116601; H117049"
    }
  ]
}