{
  "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-0122-2019",
      "product_description": "Affixus  Hip Fracture Nail 125 9 mm x 180 mm, Item Number 814309180    Product Usage:  Intended for the fixation of fractures",
      "product_quantity": "153",
      "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: 177820  177830  177890  177910  177920  244120  287770"
    }
  ]
}