{
  "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": "Terminated",
      "city": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91090",
      "recalling_firm": "ARROW INTERNATIONAL Inc.",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "N/A",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distributor in states of: FL, GA, KY, OH, PA and WV.",
      "recall_number": "Z-0351-2023",
      "product_description": "Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer",
      "product_quantity": "80 units",
      "reason_for_recall": "There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit.",
      "recall_initiation_date": "20221027",
      "center_classification_date": "20221209",
      "termination_date": "20241007",
      "report_date": "20221221",
      "code_info": "UDI/DI 10801902159448, Lot Number 13F22C0349"
    }
  ]
}