{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mercedita",
      "state": "PR",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72729",
      "recalling_firm": "Zimmer Manufacturing B.V.",
      "address_1": "Turpeaux Industrial Park Rd 1 km 123.4",
      "address_2": "N/A",
      "postal_code": "00715",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution and the country of Thailand.",
      "recall_number": "Z-0449-2016",
      "product_description": "Label reading in part as: \"NexGen System, Complete Knee Solution; Reference Number 5980-37-01; Tibial Component, Precoat, Stemmed Size 3;   Lot Number:62460264.    Indicated for patients with severe knee pain and disability and is intended for mating with a UHMWPE articular surface and Zimaloy Cobalt-Chromium-Molybdenum alloy femoral component to perform knee arthroplasty.",
      "product_quantity": "179",
      "reason_for_recall": "Complaints were received from Thailand reporting that there was no white paper (Tyvek) seal on the inner package of P/N:00-5980-037-01 unit from lot #62460264",
      "recall_initiation_date": "20151202",
      "center_classification_date": "20151218",
      "termination_date": "20160916",
      "report_date": "20151230",
      "code_info": "lot #62460264"
    }
  ]
}