{
  "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 II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71721",
      "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": "Distributed Only in Puerto Rico.",
      "recall_number": "Z-2647-2015",
      "product_description": "EXTREMITY PACK  4/CS    Used by medical staff to perform surgical procedures and  patient care procedures such as wound healing, suture removals, irrigate wounds, etc.  .",
      "product_quantity": "285",
      "reason_for_recall": "Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.",
      "recall_initiation_date": "20150710",
      "center_classification_date": "20150903",
      "termination_date": "20170412",
      "report_date": "20150909",
      "code_info": "Code:9002615  Lots:  140915322 exp. 10/31/15  141015728 exp. 11/30/15  141015728 exp. 11/30/15  141216308 exp. 12/31/15  150116556 exp. 1/1/16  150518786 exp. 5/31/16"
    }
  ]
}