{
  "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": "New Kensington",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83819",
      "recalling_firm": "Xodus Medical Inc",
      "address_1": "702 Prominence Dr",
      "address_2": "N/A",
      "postal_code": "15068-7052",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the States of : CA, ID, IL, LA, MD, NY, OH, OK, TX, VA, WI and OUS: Malaysia, Kuwait, Australia, Canada, UAE, Ireland, Korea, Saudi Arabia, Japan, Mexico",
      "recall_number": "Z-0151-2020",
      "product_description": "Cautery Tip Cleaner  REF: 30500    Product Usage:  electrosurgical accessory",
      "product_quantity": "255,000 each",
      "reason_for_recall": "The sterile barrier of some devices may have been affected",
      "recall_initiation_date": "20190919",
      "center_classification_date": "20191016",
      "termination_date": "20240304",
      "report_date": "20191023",
      "code_info": "Lot # 16DEC19 17JAN06 17JAN06A 17JAN23 17FEB27 17MAR13 17MAR13A 17APR03 17APR14 17MAY24 17MAY24A 17MAY24B 17JUN27 17JUL17 17AUG01 17SEP22 17SEP22A 17OCT23 17NOV27 17NOV27A 17DEC15 18JAN19 18JAN19A 18FEB16 18MAR02 18MAR19 18MAR19A  ***Updated 11/9/21*** 19MAR14  UDI: Case   20787551000577 and Each   00787551000573"
    }
  ]
}