{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92850",
      "recalling_firm": "ARROW INTERNATIONAL Inc.",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2591-2023",
      "product_description": "Arrow ErgoPack, Pressure Injectable Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percutaneous, implanted, long-term intravascular catheter",
      "product_quantity": "177 units",
      "reason_for_recall": "This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.",
      "recall_initiation_date": "20230810",
      "center_classification_date": "20230915",
      "report_date": "20230927",
      "code_info": "Batch/Lot number 13F22E0359",
      "more_code_info": ""
    }
  ]
}