{
  "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-0131-2019",
      "product_description": "Affixus Hip Fracture Nail 125 11mm x 180mm, Item Number 814311180  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: 129900  129910  178050  178060  178070  287720  287740"
    }
  ]
}