{
  "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": "Ongoing",
      "city": "Bristol",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85373",
      "recalling_firm": "Gentell, Inc",
      "address_1": "2701 Bartram Rd",
      "address_2": "N/A",
      "postal_code": "19007-6810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distributions and the country of South Africa.",
      "recall_number": "Z-1909-2020",
      "product_description": "Gentell Honey Hydrogel 4\"x8\" Saturated Gauze- A hydrating wound dressing containing hydrogel and honey (100% Leptospermum honey), Model  Number: GEN-11830 - Product Usage: Use Gentell Honey Hydrogel on wounds with little or no exudate, diabetic skin ulcers, venous stasis ulcers, first and second-degree burns, post-surgical incisions, cuts and abrasions.",
      "product_quantity": "4,348",
      "reason_for_recall": "During an FDA audit, it was discovered that the product was not properly registered with FDA.",
      "recall_initiation_date": "20200326",
      "center_classification_date": "20200506",
      "report_date": "20200513",
      "code_info": "Lot Numbers:  1133718  1135318  1101019  1102819  1110619  1116219  1118219  1121119  1122119  1123519",
      "more_code_info": ""
    }
  ]
}