{
  "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": "2026-04-15",
    "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": "77232",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "address_2": "N/A",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) and Canada",
      "recall_number": "Z-2327-2017",
      "product_description": "Arterial Catheterization Kit,   Arterial Line Kit with Sharps Safety Features  wire, guide, catheter  The Arrow Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels",
      "product_quantity": "27, 485 distributed in the U.S, 4,371 distributed Internationally",
      "reason_for_recall": "Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.",
      "recall_initiation_date": "20170509",
      "center_classification_date": "20170612",
      "termination_date": "20180917",
      "report_date": "20170621",
      "code_info": "Material number: ASK-04018-CC, ASK-04510-HUM, ASK-04550-UHC,     Device Listing D025180"
    }
  ]
}