{
  "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-2333-2017",
      "product_description": "1) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit  2) ARROWg+ard Blue PSI Kit  3) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit  4) ARROWg+ard Blue PSI Kit  The MACTM two-Lumen Central Venous Access Device with ARROWg+ard Blue permits venous access and catheter introduction to the central circulation. It may be inserted into the jugular, subclavian, or femoral veins",
      "product_quantity": "27,485 untis distributed in U.S., 4,371 units 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: CDA-21242-1A, CDA-29803-1A, CDC-21242-1A, CDC-29803-1A, CDC-29903-1A    Device Listing D025768"
    }
  ]
}