{
  "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": "Rock Hill",
      "address_1": "481 Lakeshore Pkwy",
      "reason_for_recall": "Micro holes were detected in the laminate of the sterile barrier system of sterilized Hartmann Econolux and Hartmann Sterilux gauze products",
      "address_2": "",
      "product_quantity": "Lot 102147399 - 421 Cases; Lot 102250396 - 360 Cases; 200105390 - 522 Cases; 200206394 - 390 Cases",
      "code_info": "Item # 56910000 (Sterilux): 102147399, 102250396, 200105390, 200206394",
      "center_classification_date": "20120622",
      "distribution_pattern": "Nationwide distribution: USA including states of: AZ, CA, FL, GA, KY, MO, MS, NC, PA, SC, TN, TX, and VA.",
      "state": "SC",
      "product_description": "Hartmann Sterilux  Ref 56910000 Sterile Premium gauze sponge  4\"x4\" 12-ply   24 boxes/case  1200 total sponges    For use in wound cleansing, debriding of wounds, wound packing, covering and swabbing",
      "report_date": "20120704",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hartmann USA, Inc",
      "recall_number": "Z-1858-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "61899",
      "termination_date": "20141006",
      "more_code_info": "",
      "recall_initiation_date": "20120514",
      "postal_code": "29730-4205",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}