{
  "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-0248-2015",
      "product_description": "Utility Drape End Product, Catalog number 900-582.    Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.",
      "product_quantity": "9700",
      "reason_for_recall": "Customed products are being recalled because of 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:   112051996  112114535  113025779  113078335  113099443  140111073  140412695  140613606  140714299"
    }
  ]
}