{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cleveland",
      "state": "OH",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96697",
      "recalling_firm": "Centerline Biomedical Inc",
      "address_1": "10000 Cedar Ave",
      "address_2": "N/A",
      "postal_code": "44106-2119",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "US distribution to states of:  Pennsylvania, Florida, Texas, New York, North Carolina, New Mexico, Virginia, Tennessee",
      "recall_number": "Z-1760-2025",
      "product_description": "Centerline Biomedical IOPS Guidewire 2, REF ATW-2; Sensorized wire used to navigate through vasculature to facilitate placement of a catheter",
      "product_quantity": "80 units",
      "reason_for_recall": "Centerline Biomedical has determined that the coating on the guidewires for lot 2404-2005 may delaminate during use of the guidewire.",
      "recall_initiation_date": "20250411",
      "center_classification_date": "20250519",
      "report_date": "20250528",
      "code_info": "UDI/DI 00843152102037, Lot Number 2404-2005"
    }
  ]
}