{
  "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": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66413",
      "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": "Worldwide Distribution - USA (nationwide) including IN, NY, WA, NE, MD, TX, AL, MI, and Internationally to Canada.",
      "recall_number": "Z-0406-2014",
      "product_description": "Synthes 2.4 mm LC-DCP Plate 6 Holes/51mm    Product Usage:  Intended for fractures, osteotomies, and replantations of small bones including the foot, ankle, and hand.",
      "product_quantity": "13",
      "reason_for_recall": "A complaint was reported regarding a screw being found in a package labeled for 2.4 mm LC-DCP Plate.",
      "recall_initiation_date": "20130730",
      "center_classification_date": "20131126",
      "termination_date": "20150817",
      "report_date": "20131204",
      "code_info": "Part No. 249.926, lot No. 8093100"
    }
  ]
}