{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "Product complaints indicated that the part and lot numbers on the packaging differed from the physical product inside the packaging.  Risk of delay in surgery.",
      "address_2": "",
      "product_quantity": "19",
      "code_info": "Item XL-200152  Lot 339260  UDI (01)00880304491366(17)210713(10)339260",
      "center_classification_date": "20170113",
      "distribution_pattern": "USA (nationwide) and Internationally to ARGENTINA",
      "state": "IN",
      "product_description": "Active Articulation ArComXL Polyethylene Bearings  Active Articulation ArComXL Bearings item XL-200152",
      "report_date": "20170125",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1025-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75970",
      "termination_date": "20170919",
      "more_code_info": "",
      "recall_initiation_date": "20161219",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}