{
  "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-2549-2015",
      "product_description": "SUTURE REMOVAL KIT CUSTOMED 100/CS   Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.",
      "product_quantity": "20200 kits",
      "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": "Catalog number: 900010  Lots:  141015851 exp. 10/31/2015  150116710 exp.1/31/2016  150117001 exp.2/28/2016  150317560 exp.3/31/2016  150317560 exp.3/31/2016  150418252 exp.5/31/2016  150418252 exp.5/31/2016  150518605 exp.5/31/2016  150518605 exp.5/31/2016"
    }
  ]
}