{
  "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": [
    {
      "status": "Terminated",
      "city": "Fajardo",
      "state": "PR",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69448",
      "recalling_firm": "Customed, Inc",
      "address_1": "Calle Igualdad Final #7",
      "address_2": "N/A",
      "postal_code": "00738",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to Florida, New York and Puerto Rico..",
      "recall_number": "Z-0336-2015",
      "product_description": "General Line Full Body Drape, catalog #900-2262    Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.",
      "product_quantity": "308",
      "reason_for_recall": "Significant compromised sterility, not limited to potentially damaged packaging.  Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.",
      "recall_initiation_date": "20141008",
      "center_classification_date": "20141128",
      "termination_date": "20170814",
      "report_date": "20141210",
      "code_info": "Lot numbers  140312128  140412652  140613722  140714242  140814776"
    }
  ]
}