{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Salisbury",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94394",
      "recalling_firm": "Andover Healthcare Inc.",
      "address_1": "9 Fanaras Dr",
      "address_2": "N/A",
      "postal_code": "01952-1444",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, CO, GA, IA, IN, OH, MN, NC, PA, TX, VA, WA.",
      "recall_number": "Z-1828-2024",
      "product_description": "Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage, Tan, 4INx5YD (5400S)",
      "product_quantity": "108 cases (1,944 individual product packages)",
      "reason_for_recall": "A packaging seal gap could impact the sterility of the product.",
      "recall_initiation_date": "20240402",
      "center_classification_date": "20240515",
      "report_date": "20240522",
      "code_info": "Model Number: 5400S; UDI/DI: 10724004641072; Batch 0031151359, Lot 10009897233."
    }
  ]
}