{
  "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": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72521",
      "recalling_firm": "Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution.  US nationwide including IA, UT, MN, PA, MO, OK, IL, OH, and WA; CANADA, and NETHERLANDS",
      "recall_number": "Z-0650-2016",
      "product_description": "Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo),  9mm, 11mm, 13mm, 15mm, and 17mm",
      "product_quantity": "21",
      "reason_for_recall": "PMMA is listed as a material on the label but the product does not contain PMMA.",
      "recall_initiation_date": "20151117",
      "center_classification_date": "20160113",
      "termination_date": "20160705",
      "report_date": "20160120",
      "code_info": "Part #11-162709   9mm  Lots: 329750, 404380, 487400, 767120, 951680  Part # 11-162711  11mm  Lots: 329760, 505030, 505050  Part # 11-162713  13mm  Lots: 837750, 977460  Part # 11-162715  15mm  772410, 837780, 897070, 951810  Part # 11-162717  17mm  Lots: 311410, 410500, 535530, 712800, 728080, 829580"
    }
  ]
}