{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Wilsonville",
      "address_1": "25999 Sw Canyon Creek Rd",
      "reason_for_recall": "The XGAUZE Trauma Dressing was recalled because the packages may acquire small tears or pinholes during shipping due to use of shipping containers that lacked adequate protective materials.  If present, these small tears or pinholes may disrupt package integrity and render the device unsterile.",
      "address_2": "",
      "product_quantity": "5004 units",
      "code_info": "Lot ESO54391, Expiration Date 9/25/2020;  Lot ESO54725, Expiration Date 3/18/2020;  Lot ESO54726, Expiration Date 3/30/2020;  Lot ESO54741, Expiration Date   4/6/2020;  Lot ESO54742, Expiration Date 4/13/2020;  Lot ESO54743, Expiration Date 4/16/2020;  Lot ESO54744, Expiration Date 4/23/2020;",
      "center_classification_date": "20150911",
      "distribution_pattern": "US Distribution to the states of : Arizona, Idaho, North Carolina, Tennessee and Virginia.",
      "state": "OR",
      "product_description": "XGAUZE Trauma Dressing, catalog number FIN-0002-01.    XGAUZE is a 3\" x 36\" z-folded rayon/polyester dressing embedded with individual compressed cellulose sponges. Upon contact with blood or exudate, the sponges expand, thus increasing the dressing's capacity to absorb fluids.     XGAUZE is packed in a pre-formed sterile barrier system (pouch sealed on three sides); one side is a PET/foil/PE film, and the other side is a PET/aluminum oxide/PE film. Packages are vacuum sealed and terminally sterilized via gamma radiation.",
      "report_date": "20150923",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Revmedx Inc",
      "recall_number": "Z-2762-2015",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "72019",
      "termination_date": "20150917",
      "more_code_info": "",
      "recall_initiation_date": "20150812",
      "postal_code": "97070-9677",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}