{
  "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": "2026-04-01",
    "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": "81038",
      "recalling_firm": "Zimmer 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 in the states of: AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WY.    The products were distributed to the following foreign countries:  Chile, Netherlands.",
      "recall_number": "Z-0163-2019",
      "product_description": "Affixus Hip Fracture Nail Right 130 13 mm x 360 mm, Item Number 814513360    Product Usage:  Intended for the fixation of fractures",
      "product_quantity": "50",
      "reason_for_recall": "There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.",
      "recall_initiation_date": "20180808",
      "center_classification_date": "20181017",
      "termination_date": "20200730",
      "report_date": "20181024",
      "code_info": "Lot Numbers: 436470  616630  616640"
    }
  ]
}