{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Roswell",
      "address_1": "1400 Holcomb Bridge Rd",
      "reason_for_recall": "The impacted product was not intended for commercial distribution to end users.",
      "address_2": "",
      "product_quantity": "32 cases",
      "code_info": "Product Code: 95221-35, Unit Code: 90372",
      "center_classification_date": "20120920",
      "distribution_pattern": "US (nationwide) including the states of CA, CO, LA, NM, OK, TX and WA.",
      "state": "GA",
      "product_description": "ULTRA Fabric Reinforced Surgical Gown, X-Large, Sterile, Test File.    The Kimberly-Clark ULTRA Fabric Reinforced Surgical Gown is a sterile, single use surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body fluids, and particulate material.",
      "report_date": "20120926",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Kimberly-Clark Corporation",
      "recall_number": "Z-2425-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62577",
      "termination_date": "20121101",
      "more_code_info": "",
      "recall_initiation_date": "20101231",
      "postal_code": "30076",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}