{
  "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-2700-2015",
      "product_description": "ORTHO-IMPLANT SURGICAL PACK,       Used by medical staff to perform surgical procedures and  patient care procedures such as wound healing, suture removals, irrigate wounds, etc.  .",
      "product_quantity": "639",
      "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:900741A  Lots:  140915516 exp. 11/30/15  150116509 exp. 12/31/15  150116510 exp. 12/31/15  150317657 exp. 3/31/16  150318094 exp. 3/31/16  150318095 exp. 3/31/16  150318197 exp. 4/30/16  150318196 exp. 4/30/16  150318198 exp. 4/30/15  150518839 exp. 5/31/16  150619189 exp. 6/30/16  150619406 exp. 6/30/16"
    }
  ]
}