{
  "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-2712-2015",
      "product_description": "C-SECTION SURGICAL PACK   2/CS       Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate",
      "product_quantity": "874",
      "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:  900921A  Lots:  141015499 exp. 3/31/16  141216451 exp. 1/31/16  141216364 exp. 12/31/15  150317861 exp. 3/31/16  150317860 exp. 3/31/16  150418472 exp. 4/30/16  150418473 exp. 4/30/16  150518583 exp. 5/31/16  150518584 exp. 5/31/16  150518913 exp. 5/31/16  150619191 exp. 6/30/16"
    }
  ]
}