{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Clearwater",
      "address_1": "1300 S. Highland Avenue",
      "reason_for_recall": "Nonapproved labeling claims (Sterile)",
      "address_2": "",
      "product_quantity": "6,491 units",
      "code_info": "ALL Lots - 11406, 11414, 12439, 12466, and 02521.",
      "center_classification_date": "20150612",
      "distribution_pattern": "Worldwide Distribution -- US, including the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WV, WY and Hawaii; and, the countries of Canada and Bahrain.",
      "state": "FL",
      "product_description": "Amerigel Hydrogel Gauze Dressing 2 x 2, A5002.    Wound Management.",
      "report_date": "20150624",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Amerx Health Care Corp.",
      "recall_number": "Z-1797-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71161",
      "termination_date": "20161003",
      "more_code_info": "",
      "recall_initiation_date": "20150225",
      "postal_code": "33756",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}