{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67834",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Road",
      "address_2": "N/A",
      "postal_code": "19605",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution including the states of  IA, OR, WV, MI, AZ, IL, PA, GA, DE, NC, LA, and VA.",
      "recall_number": "Z-1507-2014",
      "product_description": "Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheter, catalogue number  AK-45854-CDC.",
      "product_quantity": "170",
      "reason_for_recall": "Arrow is recalling the Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheter due to a labeling inconsistency. One portion of  the lidstock states that the kit contains 8.5FR x 16CM catheter, while the rest of the lidstock  correctly identifies the catheter as 8.5FR x 20CM",
      "recall_initiation_date": "20130717",
      "center_classification_date": "20140424",
      "termination_date": "20150602",
      "report_date": "20140430",
      "code_info": "lot RF2110924",
      "more_code_info": ""
    }
  ]
}