{
  "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,
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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": "36",
      "code_info": "Item XL-108323  Lot 761680  UDI (01)00880304651524(17)210713(10)761680    Item XL-108223  Lot 419460  UDI (01)00880304651494(17)210713(10)419460",
      "center_classification_date": "20170113",
      "distribution_pattern": "USA (nationwide) and Internationally to ARGENTINA",
      "state": "IN",
      "product_description": "RingLoc ArComXL Highly Crosslinked Polyethylene Liners  ArComXL High Wall +3mm Liners Size 23 item XL-108323  ArComXL MaxRom +3mm Liners Size 23 item XL-108223",
      "report_date": "20170125",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1024-2017",
      "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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}