{
  "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": "2026-07-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Greensboro",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99151",
      "recalling_firm": "ConvaTec, Inc",
      "address_1": "7815 National Service Rd Ste 600",
      "address_2": "N/A",
      "postal_code": "27409-9403",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of MD, OH, IL, NC, AZ, NY, MN, TX, KS, TN, IN, DE, MI, FL, PA, CA, VA, MS, NM, GA, CO.",
      "recall_number": "Z-2677-2026",
      "product_description": "Aquacel Ag Surgical SP   REF: 413556  9cm x 15cm/3.5 in. x 6 in., Sterile R",
      "product_quantity": "4230 units",
      "reason_for_recall": "Surgical dressing  manufactured out of specification (greater thickness).",
      "recall_initiation_date": "20260608",
      "center_classification_date": "20260707",
      "report_date": "20260715",
      "code_info": "Lot/Batch: 5G00809; Primary Pack UDI: (01) 00768455130764/ Secondary Pack UDI: (01) 00768455130634/ Tertiary Pack UDI: (01) 10768455130631"
    }
  ]
}